Identity
- Trade Name
- Merocel™ FDA UDI
- Generic Name
- Non-woven gauze pad FDA UDI
- Device Name
- PACKING 400531 20PK PR BARON SINUS-PAK FDA UDI
- Model / Reference
- 400531 FDA UDI
- Description
- PACKING 400531 20PK PR BARON SINUS-PAK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20763000616933 FDA UDI
- FDA Product Code
- EFQ FDA UDINAB FDA UDI
- GMDN Term
- Non-woven gauze pad FDA UDI
Classification
- Device Class
- U FDA UDI
- Regulation Number
- 878.4014 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Height — 0.6 Centimeter FDA UDILength — 2.5 Centimeter FDA UDIWidth — 2.0 Centimeter FDA UDI
Merocel™ by Medtronic Xomed, Inc. — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI d5e3d56e-351d-4134-9379-f61884f47dbd 36 fields · synced Jun 8, 2026