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Sharn Inc PPD-AB651

by Sharn Anesthesia

Sharn Inc PPD-AB651 is a Class I device made by Sharn Anesthesia, listed in FDA GUDID since 10 Oct 2018 (UDI-DI 00817518021614), 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 Number00817518021614 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  • Withdrawn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
Arm procedure positioner, single-use
Model / Ref / Catalog
PPD-AB651
Primary DI / UDI-DI
00817518021614
FDA product code
NOD
GMDN term
Arm procedure positioner, single-use
Device class
Class I
Regulation number
878.3910
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Arm procedure positioner, single-use

Other devices from Sharn Anesthesia

See all devices from Sharn Anesthesia →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)