Identity
- Trade Name
- Critical Cover FDA UDI
- Generic Name
- Surgical hood FDA UDI
- Device Name
- Bouffant Cap, GenPro, Lightweight, Serged Seams, 21", White FDA UDI
- Model / Reference
- BO-13821-B FDA UDI
- Description
- Bouffant Cap, GenPro, Lightweight, Serged Seams, 21", White FDA UDI
Identifiers
- Catalog Number
- BO-13821-B FDA UDI
- Primary DI / UDI-DI
- 10817583020656 FDA UDI
- FDA Product Code
- FYF FDA UDI
- GMDN Term
- Surgical hood 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
No
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
Category: Surgical hood
Critical Cover by Alphaprotech, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- MEDLINE INDUSTRIES, INC. — MEDLINE INDUSTRIES, INC. · 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
- Alphaprotech, Inc.
Sources (1)
- FDA UDI 3cc2a3ba-7e14-4bee-986c-9575e9c27106 35 fields · synced Jun 6, 2026