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Bardia Leg Bag

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bardia Leg Bag FDA UDI
Generic Name
Wearable adult urine collection bag, open-ended FDA UDI
Device Name
Bardia Leg Bag, Medium (19oz) FDA UDI
Model / Reference
150107 FDA UDI
Description
Bardia Leg Bag, Medium (19oz) FDA UDI

Identifiers

Catalog Number
150107 FDA UDI
Primary DI / UDI-DI
00801741050756 FDA UDI
FDA Product Code
KNX FDA UDI
GMDN Term
Wearable adult urine collection bag, open-ended FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 19 Fluid Ounce FDA UDI

Category: Wearable adult urine collection bag, open-ended

Bardia Leg Bag by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable adult urine collection bag, open-ended.

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 a5542cd0-d3a8-45dc-b430-c9fefd00db77 36 fields · synced Jun 6, 2026