Arthrex® AR-6200

by Arthrex, Inc.

Arthrex® AR-6200 is a Class II device made by Arthrex, Inc., listed in FDA GUDID since 4 Nov 2024 (UDI-DI 00888867039001), 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	Number00888867039001 UDI-DI	Date4 Nov 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00888867039001

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Arthrex®
Generic name: Cardiac ablation system irrigation tubing set
Model / Ref / Catalog: AR-6200

Primary DI / UDI-DI: 00888867039001
FDA product code: HRX
GMDN term: Cardiac ablation system irrigation tubing set

Device class: Class II
Regulation number: 888.1100
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)