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Channel Drain

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Channel Drain FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
Channel Drain, 7mm Flat 3/4 Fluted with 4.7mm Trocar FDA UDI
Model / Reference
072216 FDA UDI
Description
Channel Drain, 7mm Flat 3/4 Fluted with 4.7mm Trocar FDA UDI

Identifiers

Catalog Number
072216 FDA UDI
Primary DI / UDI-DI
00801741049811 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Closed-wound drain, non-bioabsorbable 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

No

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
Length — 7 Millimeter FDA UDI

Category: Closed-wound drain, non-bioabsorbable

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

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

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 9599fc18-d726-42a4-b9aa-8834549347a8 36 fields · synced Jun 8, 2026