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Ritter 9A337001-850

by Midmark Corporation

Ritter 9A337001-850 is a Class I device made by Midmark Corporation, listed in FDA GUDID since 7 May 2020 (UDI-DI 00841709111426), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841709111426 UDI-DI Date7 May 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  • Withdrawn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
Ritter
Generic name
Footrest
Model / Ref / Catalog
9A337001-850
Primary DI / UDI-DI
00841709111426
FDA product code
GBB
GMDN term
Footrest
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Related devices

Category: Footrest

Similar devices

Also classified as Footrest.

Other devices from Midmark Corporation

See all devices from Midmark Corporation →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)