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Penrose Drain

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Penrose Drain FDA UDI
Generic Name
Surgical capillary wound drain, luminal, Hevea-latex FDA UDI
Device Name
Penrose Drain 18" (457.20mm), X-Ray Opaque Rubber, 1/4" (6.35mm) FDA UDI
Model / Reference
0918010 FDA UDI
Description
Penrose Drain 18" (457.20mm), X-Ray Opaque Rubber, 1/4" (6.35mm) FDA UDI

Identifiers

Catalog Number
0918010 FDA UDI
Primary DI / UDI-DI
00801741051302 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Surgical capillary wound drain, luminal, Hevea-latex FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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 — 18 Inch FDA UDI

Category: Surgical capillary wound drain, luminal, Hevea-latex

Penrose Drain by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical capillary wound drain, luminal, Hevea-latex.

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 c68b9544-27c6-4405-b350-d021436d5840 37 fields · synced May 31, 2026