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Lightning 01

by Wenzhou Kangshun Medical Devices CO., LTD GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975185470358 UDI-DIDate8 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Lightning
Generic Name
Aneroid manual sphygmomanometer
Model / Reference
01
Primary DI / UDI-DI
06975185470358
510(k) Number
FDA Product Code
DXQ
GMDN Term
Aneroid manual sphygmomanometer
Device Class
Class II
Regulation Number
870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K230859)

Other devices from Wenzhou Kangshun Medical Devices CO., LTD

See all devices from Wenzhou Kangshun Medical Devices CO., LTD →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No