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Bard® Rectal Tube

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bard® Rectal Tube FDA UDI
Generic Name
Rectal/colonic irrigation nozzle, single-use FDA UDI
Device Name
Bard® Rectal Tube FDA UDI
Model / Reference
0006520 FDA UDI
Description
Bard® Rectal Tube FDA UDI

Identifiers

Catalog Number
0006520 FDA UDI
Primary DI / UDI-DI
00801741045981 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Rectal/colonic irrigation nozzle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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 — 20 Inch FDA UDI
Catheter Gauge — 18 French FDA UDI

Category: Rectal/colonic irrigation nozzle, single-use

Bard® Rectal Tube by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rectal/colonic irrigation nozzle, single-use.

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 9ae006b1-5cb3-4927-9fdc-a05f38ba7f14 36 fields · synced May 31, 2026