Ans Medical UP220

by Cardinalhealth

Ans Medical UP220 (MS71175) is a Class I device made by Cardinalhealth, listed in FDA GUDID since 17 May 2023 (UDI-DI 10884521738362), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10884521738362 UDI-DI	Date17 May 2023Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 10884521738362

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Ans Medical
Generic name: Patient medical adhesive remover
Model / Ref / Catalog: UP220, MS71175

Primary DI / UDI-DI: 10884521738362
FDA product code: KOX
GMDN term: Patient medical adhesive remover

Device class: Class I
Regulation number: 878.4730
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Over-the-counter
Premarket exempt
Lot / batch number

Other properties (11, all answered No)