Identity
- Trade Name
- Merocel® FDA UDI
- Generic Name
- Retractor cover FDA UDI
- Device Name
- RETRACTOR COVER 400256 10PK SELF STICK FDA UDI
- Model / Reference
- 400256 FDA UDI
- Description
- RETRACTOR COVER 400256 10PK SELF STICK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20681490104849 FDA UDI
- FDA Product Code
- LYA FDA UDI
- GMDN Term
- Retractor cover FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4780 FDA UDI
- Commercial Distribution
- Not 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
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
Dimensions & Sizes
- Size
- Length — 220.0 Millimeter FDA UDIWidth — 84.0 Millimeter FDA UDI
Merocel® by Medtronic Xomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI ef229c18-b527-43ab-a111-427124fb89f5 36 fields · synced May 31, 2026