Gav 2.0 FX220T

Gav 2.0 FX220T is a Class II device made by Aesculap AG, listed in FDA GUDID since 4 Mar 2020 (UDI-DI 04041906500160), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04041906500160 UDI-DI	Date4 Mar 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04041906500160

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Gav 2.0
Generic name: Cerebrospinal fluid shunt valve
Model / Ref / Catalog: FX220T

Primary DI / UDI-DI: 04041906500160
FDA product code: JXG
GMDN term: Cerebrospinal fluid shunt valve

Device class: Class II
Regulation number: 882.5550
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Implantable
Prescription use
Serial number
Expiration date

Other properties (9, all answered No)