Cure Medical K2

by Convatec, Purchasing Department

Cure Medical K2 is a Class II device made by Convatec, Purchasing Department, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00815947020475), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00815947020475 UDI-DI	Date24 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00815947020475

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Cure Medical
Generic name: Urethral catheterization support kit, urinary drainage
Model / reference: K2

Primary DI / UDI-DI: 00815947020475
FDA product code: OHR
GMDN term: Urethral catheterization support kit, urinary drainage

Device class: Class II
Regulation number: 876.5130
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)