Identity
- Trade Name
- REPEL FDA UDI
- Generic Name
- Glove liner FDA UDI
- Device Name
- REPEL LITE CUT REST SURGICAL GLV LNRS MED FDA UDI
- Model / Reference
- 5200-32-000 FDA UDI
- Description
- REPEL LITE CUT REST SURGICAL GLV LNRS MED FDA UDI
Identifiers
- Catalog Number
- 520032000 FDA UDI
- Primary DI / UDI-DI
- 10603295326328 FDA UDI
- FDA Product Code
- LYU FDA UDI
- GMDN Term
- Glove liner FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Glove liner
Repel by Depuy Orthopaedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Glove liner.
- GLOVE LINER — George Glove Company, Inc. · Class I
- FlexGard — LDI Solutions, LLC · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- FlexGard — LDI Solutions, LLC · Class I
- FlexGard — LDI Solutions, LLC · Class I
- GLOVE LINER — George Glove Company, Inc. · Class I
- FlexGard — LDI Solutions, LLC · 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
- Depuy Orthopaedics, Inc.
Sources (1)
- FDA UDI 7aee64ca-1400-4734-be87-e7db197879eb 35 fields · synced Jun 8, 2026