Skip to content

Sharn Inc GP9400-I

by Sharn Anesthesia

Sharn Inc GP9400-I is a Class II device made by Sharn Anesthesia, listed in FDA GUDID since 10 Oct 2018 (UDI-DI 00817518021492), 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 Number00817518021492 UDI-DI Date10 Oct 2018ListedStatusListed 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  • Withdrawn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
Sharn Inc
Generic name
General-purpose patient temperature probe, single-use
Model / Ref / Catalog
GP9400-I
Primary DI / UDI-DI
00817518021492
FDA product code
FLL
GMDN term
General-purpose patient temperature probe, single-use
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose patient temperature probe, single-use

Similar devices in this category

Other devices filed under General-purpose patient temperature probe, single-use.

Other devices from Sharn Anesthesia

See all devices from Sharn Anesthesia →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)