Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Rib spreader, reusable FDA UDI
- Device Name
- PREMIE RIB SPREADER FDA UDI
- Model / Reference
- IPN005114 FDA UDI
- Description
- PREMIE RIB SPREADER FDA UDI
Identifiers
- Catalog Number
- 341312 FDA UDI
- Primary DI / UDI-DI
- 14026704919083 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Rib spreader, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Width — 1.45 Inch FDA UDILength — 2.35 Inch FDA UDI
Category: Rib spreader, reusable
Pilling by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Symmetry Burford-Finochietto — SYMMETRY SURGICAL INC. · Class I
- Gimmi — Gimmi GmbH · Class I
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 616d3556-6157-4af2-9b58-97e917553b47 36 fields · synced Jun 8, 2026