Skip to content

proSA® FV791T

by Christoph Miethke GmbH & Co. KG

proSA® FV791T is a Class II device made by Christoph Miethke GmbH & Co. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04041906134334), 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 Number04041906134334 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
proSA®
Generic name
Cerebrospinal fluid shunt valve programmer
Model / Ref / Catalog
FV791T
Primary DI / UDI-DI
04041906134334
FDA product code
JXG
GMDN term
Cerebrospinal fluid shunt valve programmer
Device class
Class II
Regulation number
882.5550
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Cerebrospinal fluid shunt valve programmer

Similar devices in this category

Other devices filed under Cerebrospinal fluid shunt valve programmer.

Other devices from Christoph Miethke GmbH & Co. KG

See all devices from Christoph Miethke GmbH & Co. KG →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)