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Progav 2.0 FX630T

by Aesculap, Inc.

Progav 2.0 FX630T is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 4 Mar 2020 (UDI-DI 04041906502607), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04041906502607 UDI-DI Date4 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Progav 2.0
Generic name
Ventriculo-peritoneal/atrial shunt
Model / Ref / Catalog
FX630T
Primary DI / UDI-DI
04041906502607
FDA product code
JXG
GMDN term
Ventriculo-peritoneal/atrial shunt
Device class
Class II
Regulation number
882.5550
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ventriculo-peritoneal/atrial shunt

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)