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Sharn Anesthesia 105607-EU

by Sharn Anesthesia

Sharn Anesthesia 105607-EU is a Class I device made by Sharn Anesthesia, listed in FDA GUDID since 27 Oct 2022 (UDI-DI 00817518022581), 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 Number00817518022581 UDI-DI Date27 Oct 2022ListedStatusListed 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  • Withdrawn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 Anesthesia
Generic name
Surgical instrument/endoscope cleaning utensil, single-use
Model / reference
105607-EU
Primary DI / UDI-DI
00817518022581
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

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Properties

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