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Cure Catheter® Closed System

FDA UDI

Class II (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
Cure Catheter® Closed System FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Closed System Single Urinary Catheterization System with Catheter Control Feature, Coudé Tip FDA UDI
Model / Reference
CBL14C FDA UDI
Description
Closed System Single Urinary Catheterization System with Catheter Control Feature, Coudé Tip FDA UDI

Identifiers

Primary DI / UDI-DI
00815947020932 FDA UDI
FDA Product Code
KOD FDA UDI
GMDN Term
Single-administration urethral drainage catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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 — 14 French FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 12fdea34-fa2e-41d6-8582-209944eff1a6 35 fields · synced May 30, 2026