Identity
- Trade Name
- HU-FRIEDY FDA UDI
- Generic Name
- Clamp jaw cover FDA UDI
- Device Name
- Silicone Tube - 4 ft long FDA UDI
- Model / Reference
- PTRTCL FDA UDI
- Description
- Silicone Tube - 4 ft long FDA UDI
Identifiers
- Catalog Number
- PTRTCL FDA UDI
- Primary DI / UDI-DI
- 10889950020705 FDA UDI
- FDA Product Code
- KBN FDA UDI
- GMDN Term
- Clamp jaw cover FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
No
FDA UDI
Over-the-Counter
No
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
Moist Heat or Steam Sterilization FDA UDI
Category: Clamp jaw cover
Hu-Friedy by Hu-Friedy Mfg Co., Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Clamp jaw cover.
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- Fibra / Fibra® CLAMP INSERTS — APPLIED MEDICAL RESOURCES CORP. · Class II
- STEALTH® FIBRA® CLAMP INSERTS — APPLIED MEDICAL RESOURCES CORP. · Class II
- STEALTH® CLAMP INSERT — APPLIED MEDICAL RESOURCES CORP. · Class II
- STEALTH® CLAMP INSERT — APPLIED MEDICAL RESOURCES CORP. · Class II
- Soft/Soft Clamp Inserts — APPLIED MEDICAL RESOURCES CORP. · Class II
- STEALTH® CLAMP INSERTS — APPLIED MEDICAL RESOURCES CORP. · Class II
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 |
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Manufacturer
- Manufacturer
- Hu-Friedy Mfg Co., Llc
Sources (1)
- FDA UDI d4e19564-a2e5-41f0-b605-2e1db012b3bd 35 fields · synced May 29, 2026