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SEER Light Connect

by Suzuken Co., Ltd.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840682108249 UDI-DI Date15 Jun 2016ListedStatusListed 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  • Withdrawn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

Trade Name
Seer
Generic Name
Electrocardiographic ambulatory recorder
Model / Reference
Light Connect
Primary DI / UDI-DI
00840682108249
FDA Product Code
MWJ
GMDN Term
Electrocardiographic ambulatory recorder
Device Class
Class II
Regulation Number
870.2800
GUDID distribution status
Not in Commercial Distribution

Other devices from Suzuken Co., Ltd.

See all devices from Suzuken Co., Ltd. →

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No