← Back to catalogue

Bard® CritiCore® Face Shield

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® CritiCore® Face Shield FDA UDI
Generic Name
Urine monitoring system FDA UDI
Device Name
Bard® CritiCore® Face Shield FDA UDI
Model / Reference
000002FS FDA UDI
Description
Bard® CritiCore® Face Shield FDA UDI

Identifiers

Catalog Number
000002FS FDA UDI
Primary DI / UDI-DI
00801741137525 FDA UDI
FDA Product Code
EXS FDA UDI
GMDN Term
Urine monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Urine monitoring system

Bard® CritiCore® Face Shield by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI ad3c7b67-76b8-40c8-ba38-712e8042039a 35 fields · synced May 30, 2026