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Bard® CritiCore® Collection Container

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® CritiCore® Collection Container FDA UDI
Generic Name
Urine monitoring system FDA UDI
Device Name
Bard® CritiCore® Collection Container FDA UDI
Model / Reference
153200 FDA UDI
Description
Bard® CritiCore® Collection Container FDA UDI

Identifiers

Catalog Number
153200 FDA UDI
Primary DI / UDI-DI
00801741019357 FDA UDI
FDA Product Code
FFG 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

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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine monitoring system

Bard® CritiCore® Collection Container 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

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI dc5b7f51-7583-41ee-9f88-6278c7eb8ac3 35 fields · synced Jun 8, 2026