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Conmed 9840

by Conmed Corporation

Conmed 9840 is a Class I device made by Conmed Corporation, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854026199), 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 Number10845854026199 UDI-DI Date24 Sep 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  • Withdrawn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
Conmed
Generic name
Intraoperative freestanding patient positioning frame
Model / Ref / Catalog
9840
Primary DI / UDI-DI
10845854026199
FDA product code
HST
GMDN term
Intraoperative freestanding patient positioning frame
Device class
Class I
Regulation number
888.5850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Intraoperative freestanding patient positioning frame

Similar devices

Also classified as Intraoperative freestanding patient positioning frame.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)