Skip to content

Sharn Inc 105604

by Sharn Anesthesia

Sharn Inc 105604 is a Class I device made by Sharn Anesthesia, listed in FDA GUDID since 29 Apr 2021 (UDI-DI 00817518022215), 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 Number00817518022215 UDI-DI Date29 Apr 2021ListedStatusListed 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  • Withdrawn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
Surgical instrument/endoscope cleaning utensil, single-use
Model / reference
105604
Primary DI / UDI-DI
00817518022215
FDA product code
MNL
GMDN term
Surgical instrument/endoscope cleaning utensil, single-use
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument/endoscope cleaning utensil, single-use

Similar devices in this category

Other devices filed under Surgical instrument/endoscope cleaning utensil, single-use.

Other devices from Sharn Anesthesia

See all devices from Sharn Anesthesia →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)