Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- ENT soft-tissue cutting forceps FDA UDI
- Device Name
- PUNCH ANTRUM RIGHT DOWN FDA UDI
- Model / Reference
- IPN021779 FDA UDI
- Description
- PUNCH ANTRUM RIGHT DOWN FDA UDI
Identifiers
- Catalog Number
- P27843 FDA UDI
- Primary DI / UDI-DI
- 14026704809308 FDA UDI
- FDA Product Code
- KAW FDA UDI
- GMDN Term
- ENT soft-tissue cutting forceps 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
Yes
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
Moist Heat or Steam Sterilization FDA UDI
Category: ENT soft-tissue cutting forceps
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Teleflex Incorporated
Sources (1)
- FDA UDI 975e4505-7f67-49a7-a945-85df23c9b4fb 35 fields · synced Jun 1, 2026