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DMS 300-2 Holter Recorder

by Dm Systems (Beijing) Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975817741030 UDI-DIDate30 Sep 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  • Withdrawn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 23 Oct 2026.

Specification

GUDID

Generic Name
Electrocardiographic ambulatory recorder
Model / Ref / Catalog
DMS 300-2, DMS 300-2 Holter Recorder
Primary DI / UDI-DI
06975817741030
510(k) Number
FDA Product Code
MWJ
GMDN Term
Electrocardiographic ambulatory recorder
Device Class
Class II
Regulation Number
870.2800
GUDID distribution status
In Commercial Distribution

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

  • 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
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No