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Enema Ring: Fluid Collection Device

FDA UDI

Class II (US FDA UDI)

by Bracco Diagnostics Inc.

Identity

Trade Name
Enema Ring: Fluid Collection Device FDA UDI
Generic Name
Faecal incontinence collector, catheterization FDA UDI
Device Name
Barium Enema Ring FDA UDI
Model / Reference
901101 FDA UDI
Description
Barium Enema Ring FDA UDI

Identifiers

Catalog Number
901101 FDA UDI
Primary DI / UDI-DI
10815112020955 FDA UDI
FDA Product Code
FGD FDA UDI
GMDN Term
Faecal incontinence collector, catheterization 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

Category: Faecal incontinence collector, catheterization

Enema Ring: Fluid Collection Device by Bracco Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal incontinence collector, catheterization.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fdfa0aa-45f3-4146-aa2c-350d495e8732 35 fields · synced Jun 6, 2026