← Back to catalogue

Davol Bile Bag, Regular

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Davol Bile Bag, Regular FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
Bile Bag FDA UDI
Model / Reference
0015850 FDA UDI
Description
Bile Bag FDA UDI

Identifiers

Catalog Number
0015850 FDA UDI
Primary DI / UDI-DI
00801741011610 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 9.5 Inch FDA UDI
Total Volume — 19 Fluid Ounce FDA UDI

Category: Closed-wound/centesis drainage receptacle

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

Similar devices

Also classified as Closed-wound/centesis drainage receptacle.

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 15a36462-2797-486b-9479-e42d82f3b639 36 fields · synced May 30, 2026