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Cure Catheter

FDA UDI

Class II (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
CURE CATHETER FDA UDI
Generic Name
Single-administration urethral catheterization kit, single-use FDA UDI
Device Name
Hydrophilic, Male, 16”, Straight Tip, Kit FDA UDI
Model / Reference
HM12UK FDA UDI
Description
Hydrophilic, Male, 16”, Straight Tip, Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00815947021168 FDA UDI
FDA Product Code
OHR FDA UDI
GMDN Term
Single-administration urethral catheterization kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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
Catheter Gauge — 12 French FDA UDI
Length — 41 Centimeter FDA UDI

Category: Single-administration urethral catheterization kit, single-use

Cure Catheter by Convatec, Purchasing Department — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-administration urethral catheterization kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fabe163a-4ecb-4c78-b5ec-1559ec4e8e6f 35 fields · synced Jun 8, 2026