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Acumed Hr-0822-S

by Acumed LLC

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 Number10806378069536 UDI-DI Date24 Oct 2015ListedStatusListed 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  • Withdrawn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
Acumed
Generic Name
Humerus intramedullary nail
Model / Reference
HR-0822-S
Primary DI / UDI-DI
10806378069536
FDA Product Code
HSB
GMDN Term
Humerus intramedullary nail
Device Class
Class II
Regulation Number
888.3020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Humerus intramedullary nail

Other devices from Acumed LLC

See all devices from Acumed LLC →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number

Other properties (9)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No