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SEER Light Patient Cable 3CH IEC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04987382233942 UDI-DI Date6 Oct 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  • Withdrawn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
Electrocardiograph, professional, multichannel
Model / Reference
SEER Light Patient Cable 3CH IEC
Primary DI / UDI-DI
04987382233942
FDA Product Code
MWJ
GMDN Term
Electrocardiograph, professional, multichannel
Device Class
Class II
Regulation Number
870.2800
GUDID distribution status
Not in Commercial Distribution

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See all devices from Suzuken Co., Ltd. →

Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • 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
  • Expiration Date: No