ICU Medical 011-MC100Recalls & reported problems

Summary

The FDA's MAUDE database contains 93 adverse event reports that list this exact device (DI 00840619042509), received between Dec 1, 2017 and Sep 17, 2026 — classified as 1 death, 92 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (51 reports).

52 other recalls cover devices cleared under the same FDA submission (K970855); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 93 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 17, 2026No Flow

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50809812 ↗
• MalfunctionSep 17, 2026Obstruction of Flow

  The event involved Micro Clave Clear Connector. It was reported that the silicone seal at the connection point inside the housing became jammed, obstructing the flow path and preventing the IV from entering. There was patient involvement but no harm.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50803794 ↗
• MalfunctionSep 1, 2026Backflow

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50544747 ↗
• MalfunctionApr 30, 2026Fluid/Blood Leak

  THE EVENT OCCURRED ON AN UNSPECIFIED DATE AND INVOLVED A MICROCLAVE® CLEAR CONNECTOR. DURING THE EARLY SHIFT, THE IV LINE REPORTEDLY LEAKED INTO THE BED BECAUSE THE CLAVE DEVICE WAS VISIBLY DAMAGED. THE PATIENT WAS RECEIVING INFUSION OF ELECTROLYTES AND GLUCOSE. AT THE TIME OF THE ISSUE. THE PATIENT REQUIRED A BLOOD GAS CHECK TO CHECK FOR HYPOGLYCEMIA. THE PATIENT IS DOING WELL. THIS IS THE ONLY CLAVE SO FAR THAT HAS BEEN FOUND TO BE DEFECTIVE. THERE ARE NO OTHER DETAILS AVAILABLE REGARDING THIS COMPLAINT/EVENT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25044590 ↗
• MalfunctionMar 30, 2026Fluid/Blood Leak

  THE EVENT INVOLVED MICROCLAVE¿ CLEAR CONNECTOR. IT WAS REPORTED THAT AFTER INJECTING ANTIBIOTICS INTO THE CONNECTOR ALREADY IN PLACE, THE SYRINGE WAS CHANGED WHEN EMPTY. DURING THE SYRINGE CHANGE, WHEN ADDING THE RINSE SOLUTION, THE SYRINGE PLUNGERS WERE OBSERVED TO BE WET, AND DROPS WERE DRIPPING FROM THE CONNECTOR. THE DEVICE HAD BEEN INSTALLED 5 DAYS PRIOR TO THE PROBLEM/EVENT. DISINFECTION WAS CARRIED OUT WITH CHLORHEXIDINE FOR 30 SECONDS BETWEEN EACH SYRINGE CHANGE. THERE WAS NO REPORTED PATIENT INVOLVEMENT, AND PATIENT HARM OR ADVERSE EVENTS WERE UNKNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24737019 ↗
• MalfunctionMar 13, 2026Fluid/Blood Leak

  AN EVENT OCCURRED INVOLVING A MICROCLAVE¿ CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT AFTER HOME TREATMENT WITH A PATIENT RECEIVING CHEMOTHERAPY DRUG 5-FLUOROURACIL (5-FU) AND THE CADD VIP INFUSION PUMP, THE PATIENT RETURNED WITH LEAKAGE OBSERVED BETWEEN THE CONNECTION OF THE EXTENSION OF THE 100 ML CASSETTE AND THE MICROCLAVE, WHICH WAS PLACED ON THE LUER LOCK CONNECTION TO SEAL THE CASSETTE. ADDITIONALLY, IT WAS NOTED THAT 5-FU HAD SOLIDIFIED IN THE TRANSPORT BAG AND AT THE CONNECTION BETWEEN THE MICROCLAVE AND THE CASSETTE EXTENSION. THERE WAS PATIENT INVOLVEMENT, AND NO DELAY IN THERAPY; HARM WAS NOT REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24598408 ↗
• MalfunctionMar 7, 2026Fluid/Blood Leak

  THE EVENT INVOLVED A MICROCLAVE CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT THE MICROCLAVE WAS CONNECTED TO SECONDARY LINE 011-CH3261 WHICH CREATES AN OPEN SYSTEM AND THERE WAS A HIGH RISK CHEMO SPILL. PATIENT INVOLVEMENT WAS UNKNOWN, BUT HARM WAS NOT REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24539887 ↗
• MalfunctionMar 5, 2026Fluid/Blood Leak

  THE EVENT OCCURRED IN AN UNSPECIFIED DATE AND INVOLVED A MICROCLAVE CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT THE IV BUNG VALVE WAS NOT CLOSING, AND THE PATIENT BLED OUT FROM THE CONNECTOR. THE PRODUCT WAS NOT REPROCESSED OR RE-STERILIZED PRIOR TO USE. NO MEDICATION WAS USED WITH THE PRODUCT. SOMEONE BECAME AWARE OF THE ISSUE DURING CLINICAL OBSERVATION AT TIME. THERE WAS PATIENT INVOLVEMENT, BUT NO ONE WAS HARMED IN THE EVENT. NO MEDICATION WAS REPORTED.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 24524596 ↗
• MalfunctionFeb 24, 2026Fluid/Blood Leak

  EVENT OCCURRED REGARDING A MICROCLAVE WHERE IT WAS REPORTED THAT ON TWO OCCASIONS, AFTER CONNECTING THE PLUG TO THE VENOUS CATHETER, THE SEALING DID NOT OCCUR, AND BLOOD LEAKED THROUGH IT. THE INCIDENT OCCURRED DURING PATIENT USE; HOWEVER, NO HARM TO THE PATIENT RESULTED FROM THIS EVENT. ICU MEDICAL COMPLAINT REFERENCE: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24430395 ↗
• MalfunctionFeb 24, 2026Fluid/Blood Leak

  EVENT OCCURRED REGARDING A MICROCLAVE WHERE IT WAS REPORTED THAT AFTER CONNECTING THE PLUG TO THE VENOUS CATHETER, THE SEALING DID NOT OCCUR, AND BLOOD LEAKED THROUGH IT. THE INCIDENT OCCURRED DURING PATIENT USE; HOWEVER, NO HARM TO THE PATIENT RESULTED FROM THIS EVENT. ICU MEDICAL COMPLAINT REFERENCE: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24429767 ↗
• MalfunctionDec 18, 2025Fluid/Blood Leak; Fluid/Blood Leak

  THIS REPORT IS FOR PATIENT 1 OF 3.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23842758 ↗
• MalfunctionDec 18, 2025Fluid/Blood Leak; Fluid/Blood Leak

  AN EMAIL WAS RECEIVED REGARDING A MICROCLAVE CLEAR CONNECTOR ALLEGING A LEAK DURING PATIENT USE. IT WAS REPORTED THAT THE CLAVE IS CONNECTED VIA AN ELASTOMERIC PUMP/AUTOFUSER TO A CENTRAL VENOUS CATHETER. THE SYMPTOMS APPEAR AFTER APPROXIMATELY 4 DAYS. SYMPTOMS OF LEAKAGE, ANTIBIOTIC DEPOSITS AGAINST THE CLAVE CHAMBER, AND CONDENSATION. THERE WAS NO PATIENT HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23842723 ↗
• MalfunctionDec 18, 2025Fluid/Blood Leak; Fluid/Blood Leak

  THIS REPORT IS FOR PATIENT 3 OF 3.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23842658 ↗
• MalfunctionNov 20, 2025Disconnection; Disconnection

  THE EVENT INVOLVED A MICROCLAVE® CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT THE ADAPTOR DISLODGED WHEN IN USE. IT WAS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT; HARM WAS NOT REPORTED AS CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23607372 ↗
• MalfunctionNov 12, 2025No Flow; No Flow

  A COMPLAINT WAS RECEIVED REGARDING MICROCLAVE CLEAR CONNECTOR THAT EXPERIENCED NO FLOW. THE REPORTER STATED THE FOLLOWING:¿ THE RADIOPHARMACEUTICAL COULD NOT BE INJECTED VIA THE BIDIRECTIONAL VALVE. NO PROBLEMS WERE OBSERVED DURING DEVICE INSERTION. THIS ISSUE WAS ENCOUNTERED WITH SEVERAL VALVES FROM THE SAME BATCH, WHICH IS WHY WE QUARANTINED THE VALVES FROM THAT BATCH. A VALVE FROM ANOTHER BATCH WAS THEN USED WITHOUT INCIDENT. THERE WAS NO CONSEQUENCE FOR THE PERSONNEL.¿ THERE IS PATIENT INVOLVEMENT. THE EVENT WAS NOTICED AT THE BEGINNING OF THE INJECTION OF THE MEDICATION. THE NAME OF THE RADIOPHARMACEUTICAL MEDICATION IS NOT KNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23537120 ↗
• MalfunctionNov 3, 2025No Flow; No Flow

  EVENT OCCURRED REGARDING A MICROCLAVE¿ CLEAR CONNECTOR WHERE IT WAS REPORTED THAT THE PRODUCT WAS VENTED WITH A LUER SLIP SYRINGE, AFTER CONNECTING TO THE INFUSION THE CLAVE WAS NO LONGER PERMEABLE. THE STATUS OF THE PRODUCT AT THE TIME OF EVENT WAS DURING INFUSION. THE OPERATOR VENTED THE CONNECTOR WITH A SYRINGE. AN IV WAS THEN CONNECTED, BUT THE CONNECTOR WAS NOT FULLY OPEN, PREVENTING THE IV FROM FLOWING. THERE WAS PATIENT INVOLVEMENT, THERE WAS DELAY IN THERAPY, UNKNOWN ADVERSE EVENT AND NO HARM WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23452985 ↗
• MalfunctionOct 28, 2025Fluid/Blood Leak; Fluid/Blood Leak

  THE EVENT INVOLVED A MICROCLAVE CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT THE MICROCLAVE CONNECTOR ON THE CENTRAL VENOUS CATHETER (CVC) WAS CLOSED WITH A LIGHT GREEN CAP. DURING THE NIGHT, THE PATIENT WAS FOUND AFTER 30 MINUTES IN THIS CONDITION. THE CUSTOMER REPORTED THAT THE FOAM MATERIAL APPARENTLY REMAINED INSIDE, CAUSING BLOOD TO LEAK OUT. THE INCIDENT DID NOT RESULT IN SERIOUS CONSEQUENCES FOR THE PATIENT. THERE WAS PATIENT INVOLVEMENT BUT NO PATIENT HARM.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 23406446 ↗
• MalfunctionOct 27, 2025Fluid/Blood Leak; Fluid/Blood Leak

  EVENT OCCURRED REGARDING AN MICROCLAVE¿ CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED BLOOD LEAKAGE WITH THE CONNECTOR. THERE WAS PATIENT INVOLVEMENT BUT THERE WAS NO REPORTED PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23398028 ↗
• MalfunctionOct 21, 2025Fluid/Blood Leak; Fluid/Blood Leak

  A PATIENT REPORTEDLY BLED THROUGH A MICROCLAVE¿ CLEAR CONNECTOR DURING A CT CONTRAST IMAGING TEST PROCEDURE AT THE LOCATION OF THE PATIENT'S CANNULA AND THE MICROCLAVE. THE PRESSURE LIMIT OF 325 PSI WAS EXCEEDED (WITH NO REASON EXPLAINED), AND AS A RESULT, THE INJECTION SPEED DECREASED CONSIDERABLY AND THE IMAGING WAS NOT OPTIMAL. AFTER THE IMAGING, THE PATIENT BLED THROUGH THE MICROCLAVE, IT WAS THEN NOTICED THAT THE RUBBER PART OF THE MICROCLAVE HAD SUNK IN. ALSO, AT LEAST ON MAY 13, IT WAS NOTICED THAT FOR SEVERAL PATIENTS, THE PRESSURE LIMIT HAD BEEN EXCEEDED FOR AN UNEXPLAINED REASON, WHICH IS VERY RARE. THERE WAS NO PATIENT HARM REPORTED.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 23354206 ↗
• MalfunctionJul 31, 2025No Flow; No Flow

  ADDITIONAL INFORMATION FROM THE CUSTOMER WAS RECEIVED ON 29-JUL-2025 STATING THAT THE SAMPLE IS A MICROCLAVE CLEAR VALVE THAT THEY CURRENTLY KEEP IN THEIR OFFICE. THE SAMPLE DOES NOT CONTAIN ANY DANGEROUS MATERIAL BUT IT HAS NEVERTHELESS BEEN CONNECTED TO A CENTRAL VENOUS LINE AND THEREFORE, TRACES OF BLOOD ARE VISIBLE. NO VISIBLE DEFECTS WERE NOTED ON THE MICROCLAVE DEVICE. THE PATIENT RECOVERED. THE VALVE WAS CHANGED IMMEDIATELY AS IT IS IMPOSSIBLE TO INJECT OTHERWISE. THERE WAS DELAY IN PROCESSING BUT ACCEPTABLE BECAUSE DEFECT OF THE MATERIAL WAS PERCEIVED QUICKLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22677127 ↗
• MalfunctionJul 7, 2025Disconnection; Fluid/Blood Leak; Disconnection; Fluid/Blood Leak

  A COMPLAINT WAS RECEIVED REGARDING A MICROCLAVE® CLEAR CONNECTOR THAT EXPERIENCED LOOSE CONNECTION AND LEAKAGE. THE REPORTER STATED THAT " THE CONNECTOR DOES NOT "GRAB" THE SYRINGE ENOUGH AND THE CONTENTS SQUIRT BACK/PASS.¿ THE STATUS OF THE PRODUCT AT THE TIME OF THE EVENT WAS DURING INFUSION. IT WAS NOT DETECTED PRIOR TO DIRECT PATIENT USE. NO SERIOUS INJURY/DEATH, NO BLOOD LOSS, NO UNPROTECTED CHEMO EXPOSURE , NO DELAY IN CRITICAL THERAPY , NO ADVERSE OPERATOR CONSEQUENCES , NO MED/SURG INTERVENTION REQUIRED. THE DEVICES WERE CHANGED OUT/REPLACED WITH NO FURTHER PROBLEMS ENCOUNTERED. INVOLVED PRODUCT WAS DISPOSED BUT SAME LOT DEVICE SAMPLE IS AVAILABLE FOR INVESTIGATION. UPDATE: PROVIDING ADDITIONAL INFORMATION STATING THAT THERE WAS NO ANY DEFECTS, TEARS, OR CUTS NOTED ON THE PRODUCT. NO UNPROTECTED CHEMO EXPOSURE AND IT DID NOT COME INTO CONTACT WITH THE PATIENT OR HEALTH CARE PROVIDER. THE MEDICATION INVOLVED IS PARENTERAL NUTRITION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22430856 ↗
• MalfunctionJun 27, 2025Improper Flow or Infusion; Material Deformation; Improper Flow or Infusion; Material Deformation

  THE INTERNAL MOLD (SILICONE) OF A MICROCLAVE¿ CLEAR CONNECTOR WAS REPORTEDLY TWISTED, PREVENTING THE PROPER INTRODUCTION OF THE MEDICATION FOR THE PATIENT. THIS OCCURRED DURING NON-SPECIFIC SEDATIVE MEDICATION TREATMENT OF AN ENDOSCOPY PROCEDURE. UNSPECIFIED SYRINGE INFUSION PUMPS WITH UNSPECIFIED EXTENSION SETS WERE ALSO IN USE AT THE TIME. THE DEVICE WAS NOT SUBJECTED TO RE-STERILIZATION. THERE WAS NO DELAY IN THERAPY OR ADVERSE EVENT/HARM AS RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22348471 ↗
• MalfunctionJun 26, 2025Disconnection; Disconnection

  THE EVENT OCCURRED ON AN UNSPECIFIED DATE INVOLVING A MICROCLAVE¿ CLEAR CONNECTOR WHERE IT WAS REPORTED THAT THE CUSTOMER WAS HAVING SEVERAL DISCONNECTION PROBLEMS WITH THE LUER AND THE CATHETER. THERE WAS UNKNOWN PATIENT INVOLVEMENT AND UNKNOWN ADVERSE EVENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22341538 ↗
• MalfunctionJun 19, 2025Break; Break

  THE EVENT INVOLVED A MICROCLAVE¿ CLEAR CONNECTOR WHERE THE CUSTOMER REPORTED THAT UPON DISCONNECTING THE WHITE LUMEN DURING THE ADMINISTRATION OF BLOOD COMPONENTS THROUGH THE CENTRAL VENOUS CATHETER, A PART OF THE BIO-CONNECTOR REMAINED INSIDE AND COULD NOT BE REMOVED. IT WAS ALSO MENTIONED THAT ATTEMPTS WERE MADE TO EXTRACT THE PORTION OF THE BIO-CONNECTOR THAT REMAINED IN THE LUMEN, BUT THEY WERE UNSUCCESSFUL. ALTHOUGH THE EVENT OCCURRED DURING PATIENT USE, THERE WAS NO PATIENT HARM REPORTED AS A CONSEQUENCE OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22292848 ↗
• MalfunctionJun 16, 2025Disconnection; Disconnection

  THE EVENT INVOLVED A MICROCLAVE¿ CLEAR CONNECTOR. THE REPORTER STATED THAT THE BIOMEDICAL SYRINGES WERE BEING PUSHED OUT BY THE MICROCLAVE. THEY STATED THAT DURING USE, THE MICROCLAVE NO LONGER PERFORMED THE PROPER LOCKING MECHANISM THAT IT ALWAYS USED TO, AND THAT IT IS NOW NECESSARY TO MAINTAIN ALL THE PRESSURE IN THE PATIENT'S LINE THROUGH THE MICROCLAVE FOR DRUG ADMINISTRATION. THE REPORTER STATED THAT THE SYRINGES DISCONNECTED EVEN AFTER PERFORMING THE QUARTER TURN. NO MEDICATION WAS USED AT THE TIME OF THE EVENT. THERE WAS PATIENT INVOLVEMENT, A DELAY IN THERAPY, HOWEVER THERE WAS NO ADVERSE EVENT AND HARM AS RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22215811 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K970855. One submission often covers many models, so check the product and lot details in each record.

• Z-1722-2022 · Aug 1, 2022 · Open, Classified
  MicroClave Clear Neutral Connector; MicroClave Clear Connector; MicroClave Clear Neutral Connector, Approx Priming Volume: 0.04 mL. Accessory for Intravascular Administration S
• Z-0687-2014 · Dec 24, 2013 · Terminated
  78" Ext Set w/2 BCV-Clave, Remv 2-Gang 4-Way Stopcocks, NanoClave" T-Connector, 4 Clamps, Rotating Luer, 3 Exts, Part No. A1000, Item No. K7094-001 The ICU Needleless Connector is
• Z-0698-2014 · Dec 24, 2013 · Terminated
  30" (76 cm) Appx 3.7 ml, Ext Set w/Remv 2 Gang CLAVE Stopcock, Remv CLAVE Stopcock, NanoClave T-Connector, Rotating Luer, 1 Ext, Part No. A1000, Item No. SC124 The ICU Needleless
• Z-0675-2014 · Dec 24, 2013 · Terminated
  87" (221 cm) Appx 2.9 ml, Smallbore Trifuse Ext Set w/NanoClave, 0.2 Micron Filter, 4 Clamps, Rotating Luer, 2 Exts, Drop-In NanoClave, Part No. A1000, Item No. A1078 The ICU Needl
• Z-0671-2014 · Dec 24, 2013 · Terminated
  11" Smallbore Bifuse Ext Set w/1.2 Micron Filter, NanoClave", 3 Clamps, Rotating Luer, Part No. A1000, Item No. A1052 The ICU Needleless Connector is a single use, sterile, non-pyr
• Z-0680-2014 · Dec 24, 2013 · Terminated
  6" (15 cm) Appx 0.27 ml, Smallbore Ext Set w/Clamp, NanoClave" TConnector, Rotating Luer, Part No. A1000, Item No. K7084-001 The ICU Needleless Connector is a single use, sterile,
• Z-0692-2014 · Dec 24, 2013 · Terminated
  10" (25 cm) Appx 0.41 ml, Smallbore Ext Set w/MicroClave Clear, NanoClave", Clamp, Rotating Luer, Part No. A1000, Item No. K7101-001 The ICU Needleless Connector is a single use,
• Z-0679-2014 · Dec 24, 2013 · Terminated
  8" Ext Set w/NanoClave" Stopcock, Clamp, Rotating Luer, Part No. A1000, Item No. AC102 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use
• Z-0696-2014 · Dec 24, 2013 · Terminated
  13" Pentafuse Smallbore Ext Set w/NanoClave", 1.2 Micron Filter, 3 MicroClave Clear (Yellow, Red, Green Rings), 6 Clamps, Rotating Luer, Part No. A1000, Item No. K7106-001 The ICU
• Z-0701-2014 · Dec 24, 2013 · Terminated
  5" Smallbore Ext Set w/MicroClave T-Connector, Clamp, Rotating Luer, Item # B33101-T, Lot # 2791358. The ICU Needleless Connector is a single use, sterile, non-pyrogenic device in
• Z-0674-2014 · Dec 24, 2013 · Terminated
  10" Smallbore Pentafuse Ext Set w/5 NanoClave", 5 Clamps, Rotating Luer, Part No. A1000, Item No. A1071 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device
• Z-0683-2014 · Dec 24, 2013 · Terminated
  7" (18 cm) Appx 0.26 ml, Smallbore Ext Set w/MicroClave Clear, NThe ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intr
• Z-0706-2014 · Dec 24, 2013 · Terminated
  6" (15 cm) Appx 0.24 ml, Smallbore Ext Set w/MicroCLAVE Clear, Clamp, NanoClave T-Connector, Rotating Luer, Item # A1003, Lot # 2773812. The ICU Needleless Connector is a single u
• Z-0666-2014 · Dec 24, 2013 · Terminated
  6" (15 cm) Appx 0.26 ml, Smallbore Ext Set w/Clamp, NanoClave TConnector, Rotating Luer, Part No. A1000, Item No. A1001 The ICU Needleless Connector is a single use, sterile, non-p
• Z-0669-2014 · Dec 24, 2013 · Terminated
  8" (20 cm) Appx 0.51 ml, Smallbore Ext Set w/MicroCLAVE Clear, 0.2 Micron Filter, NanoClave T-Connector, Clamp, Rotating Luer, Part No. A1000, Item No. A1014 The ICU Needleless Con

…and 37 more.