Identity
- Trade Name
- Key Surgical Plastic Instruments FDA UDI
- Generic Name
- Towel clamp, reusable FDA UDI
- Device Name
- Plastic Instruments, Sponge Forcep, 9.5-inch, purple FDA UDI
- Model / Reference
- KS-554-50 FDA UDI
- Description
- Plastic Instruments, Sponge Forcep, 9.5-inch, purple FDA UDI
Identifiers
- Catalog Number
- KS55450 FDA UDI
- Primary DI / UDI-DI
- 00849771027867 FDA UDI
- FDA Product Code
- HXD FDA UDI
- GMDN Term
- Towel clamp, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
Key Surgical Plastic Instruments by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Key Surgical, LLC
Sources (1)
- FDA UDI eb06e3de-30b1-4f93-a88e-fee655973a64 36 fields · synced May 31, 2026