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Na 01

by wenzhou dongfang medical instrument co., ltd 2 variants

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06970784670109 UDI-DI Date20 Nov 2020ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Blood pressure cuff, reusable
Model / Reference
01
Primary DI / UDI-DI
06970784670109
FDA Product Code
LDE
GMDN Term
Blood pressure cuff, reusable
Device Class
Class I
Regulation Number
870.1875
GUDID distribution status
Not in Commercial Distribution

Other devices from wenzhou dongfang medical instrument co., ltd

See all devices from wenzhou dongfang medical instrument co., ltd →

Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No