CathAttach CA0612

by Polarseal Tapes and Conversions Limited

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

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05060419550706 UDI-DI	Date22 Apr 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: CathAttach
Generic Name: Wearable percutaneous catheter/tube holder, single-use
Model / Reference: CA0612

Primary DI / UDI-DI: 05060419550706
FDA Product Code: KMK
GMDN Term: Wearable percutaneous catheter/tube holder, single-use

Device Class: Class I
Regulation Number: 880.5210
GUDID distribution status: In Commercial Distribution

Properties

Sterile
Single Use
Prescription Use
Premarket Exempt
Lot / Batch Number
Serial Number
Expiration Date
Manufacturing Date

Other properties (6)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No