Identity
- Trade Name
- Fenwal Slide Clamp FDA UDI
- Generic Name
- Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
- Device Name
- Fenwal Slide Clamp FDA UDI
- Model / Reference
- 4R4423H FDA UDI
- Description
- Fenwal Slide Clamp FDA UDI
Identifiers
- Catalog Number
- 4R4423H FDA UDI
- Primary DI / UDI-DI
- 14086000903261 FDA UDI
- FDA Product Code
- KSS FDA UDI
- GMDN Term
- Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medical tubing clip/clamp, temporary, non-calibrated, reusable
Fenwal Slide Clamp by Fresenius Kabi — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Medical tubing clip/clamp, temporary, non-calibrated, reusable.
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Anmuth Medical International — ANMUTH MEDICAL INTERNATIONAL LLC · Class I
- Molded Products, Inc. — MOLDED PRODUCTS INC. · Class I
- FORCEPS — KLS-Martin L.P. · Class I
- Integra® Miltex® — Integra LifeSciences Production Corporation · Class I
- Molded Products, Inc. — MOLDED PRODUCTS INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- VORSE TUBE OCCLUDING CLAMP — SONTEC INSTRUMENTS, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fresenius Kabi
Sources (1)
- FDA UDI e1342652-1747-4c1f-bdba-c6d78327d7fb 35 fields · synced Jun 1, 2026