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BOEHRINGER® CareDry™ System

FDA UDI

Class I (US FDA UDI)

by Boehringer Laboratories, Llc

Identity

Trade Name
BOEHRINGER® CareDry™ System FDA UDI
Generic Name
Female wearable urinal, single-use FDA UDI
Device Name
CareDry™ System FDA UDI
Model / Reference
7665 FDA UDI
Description
CareDry™ System FDA UDI

Identifiers

Primary DI / UDI-DI
10816286021144 FDA UDI
FDA Product Code
NZU FDA UDI
GMDN Term
Female wearable urinal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 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

No

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: Female wearable urinal, single-use

BOEHRINGER® CareDry™ System by Boehringer Laboratories, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Female wearable urinal, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boehringer Laboratories, Llc

Sources (1)

  • FDA UDI a3b1f6f0-c6d3-4b36-b06c-b3829fe60cd4 34 fields · synced May 30, 2026