Conveen

FDA UDI

Class I (US FDA UDI)

by Coloplast A/S

Identity

Trade Name: Conveen FDA UDI
Generic Name: Personal device holder, reusable FDA UDI
Model / Reference: 05050 FDA UDI

Identifiers

Catalog Number: 05050 FDA UDI
Primary DI / UDI-DI: 05708932135184 FDA UDI
FDA Product Code: NNW FDA UDI
GMDN Term: Personal device holder, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 23.6 Inch FDA UDI
Length — 60 Centimeter FDA UDI

Category: Personal device holder, reusable

Conveen by Coloplast A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Coloplast A/S

Sources (1)

FDA UDI ed413522-90f1-41aa-a28f-20633a5617b0 35 fields · synced May 31, 2026