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Gentlecath Glide

FDA UDI

Class II (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
GENTLECATH GLIDE FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
GentleCath Glide Femenino CH10 FDA UDI
Model / Reference
510476 FDA UDI
Description
GentleCath Glide Femenino CH10 FDA UDI

Identifiers

Primary DI / UDI-DI
00768455168835 FDA UDI
510(k) Number
K181206 FDA UDI
FDA Product Code
GBM 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
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

Category: Single-administration urethral drainage catheter

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

Similar devices

Also classified as Single-administration urethral drainage catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9f99fa5b-63cf-4f76-bb6b-fcc203689276 35 fields · synced Jun 8, 2026