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Urocare® Standard Top Adapter

FDA UDI

Class II (US FDA UDI)

by Urocare Products, Inc.

Identity

Trade Name
Urocare® Standard Top Adapter FDA UDI
Generic Name
Open-ended wearable urine collection bag, non-sterile FDA UDI
Device Name
ADAPTOR, TOP, URINE COLLECTION, STANDARD, REUSABLE, REPLACEMENT Replacement Top Adapter for all Urocare Latex Urine Collection Leg Bags. FDA UDI
Model / Reference
6002 FDA UDI
Description
ADAPTOR, TOP, URINE COLLECTION, STANDARD, REUSABLE, REPLACEMENT Replacement Top Adapter for all Urocare Latex Urine Collection Leg Bags. FDA UDI

Identifiers

Catalog Number
6002 FDA UDI
Primary DI / UDI-DI
00792293060020 FDA UDI
FDA Product Code
KNX FDA UDI
NNW FDA UDI
GMDN Term
Open-ended wearable urine collection bag, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 1.24 Inch FDA UDI
Outer Diameter — 0.84 Inch FDA UDI
Weight — 0.01 Pound FDA UDI

Category: Open-ended wearable urine collection bag, non-sterile

Urocare® Standard Top Adapter by Urocare Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-ended wearable urine collection bag, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 91b1184c-26b8-4b6d-9132-f9a34f3848c7 36 fields · synced May 30, 2026