Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Periocular/lacrimal retractor, self-retaining FDA UDI
- Device Name
- RET/ELEV ORBITAL 16MM X 25MM 182MM LNGTH FDA UDI
- Model / Reference
- IPN912354 FDA UDI
- Description
- RET/ELEV ORBITAL 16MM X 25MM 182MM LNGTH FDA UDI
Identifiers
- Catalog Number
- P25167 FDA UDI
- Primary DI / UDI-DI
- 14026704801807 FDA UDI
- FDA Product Code
- HNI FDA UDI
- GMDN Term
- Periocular/lacrimal retractor, self-retaining FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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: Periocular/lacrimal retractor, self-retaining
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 2d10faa7-e285-46b1-8c07-9e70aa2e3022 35 fields · synced Jun 6, 2026