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Critical Cover

FDA UDI

Class I (US FDA UDI)

by Alphaprotech, Inc.

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

Similar devices

Also classified as Surgical hood.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alphaprotech, Inc.

Sources (1)

  • FDA UDI 3cc2a3ba-7e14-4bee-986c-9575e9c27106 35 fields · synced Jun 6, 2026