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Lightning Products 01

by wenzhou dongfang medical instrument co., ltd

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number06970784670703 UDI-DI Date1 Aug 2017ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Lightning Products
Generic Name
Blood pressure cuff, reusable
Model / Reference
01
Primary DI / UDI-DI
06970784670703
510(k) Number
FDA Product Code
DXQ
GMDN Term
Blood pressure cuff, reusable
Device Class
Class II
Regulation Number
870.1120
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K081951)

Show all (9)

Other devices from wenzhou dongfang medical instrument co., ltd

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Properties

  • Over-the-Counter
  • Lot / Batch Number
  • Expiration 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
  • Manufacturing Date: No