Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- ENT elevator FDA UDI
- Device Name
- Ossoff Micro Flap Elevator 2.0MM FDA UDI
- Model / Reference
- IPN925203 FDA UDI
- Description
- Ossoff Micro Flap Elevator 2.0MM FDA UDI
Identifiers
- Catalog Number
- 506836 FDA UDI
- Primary DI / UDI-DI
- 14026704742858 FDA UDI
- FDA Product Code
- KAD FDA UDI
- GMDN Term
- ENT elevator 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: ENT elevator
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 24ded5f9-f3e6-4fff-be31-2b9d5db695a0 35 fields · synced May 30, 2026