Identity
- Trade Name
- Applier, hemostatic clip FDA UDI
- Generic Name
- Open-surgery ligation clip applier FDA UDI
- Model / Reference
- PRT120-1B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03661522039823 FDA UDI
- FDA Product Code
- HBT FDA UDI
- GMDN Term
- Open-surgery ligation clip applier 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
Yes
FDA UDI
Dry Heat Sterilization FDA UDI
Applier, hemostatic clip by Peters Surgical — 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
- Peters Surgical
Sources (1)
- FDA UDI f2593e7c-fdb5-4c0d-93e7-1834cafa123e 33 fields · synced May 30, 2026