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SAEHAN Digital Hand Dynamometer(DHD-1) SH1001

by Saehan Corp.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809513720298 UDI-DI Date18 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SAEHAN Digital Hand Dynamometer(DHD-1)
Generic Name
Hand dynamometer/pinchmeter, electronic
Model / Ref / Catalog
SH1001
Primary DI / UDI-DI
08809513720298
FDA Product Code
LBB
GMDN Term
Hand dynamometer/pinchmeter, electronic
Device Class
Class II
Regulation Number
888.1240
GUDID distribution status
In Commercial Distribution

Other devices from Saehan Corp.

Properties

  • Premarket Exempt

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No