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C3 Wave SYSTEMC3 Wave System DMRC3S96

by Medical Components Inc

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 Number00884908146974 UDI-DI Date27 Aug 2019ListedStatusListed 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  • Withdrawn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
C3 Wave SYSTEMC3 Wave System
Generic Name
Central venous catheter navigation system, electrocardiographic
Model / Ref / Catalog
DMRC3S96
Primary DI / UDI-DI
00884908146974
FDA Product Code
LJS
GMDN Term
Central venous catheter navigation system, electrocardiographic
Device Class
Class II
Regulation Number
880.5970
GUDID distribution status
Not in Commercial Distribution

Other devices from Medical Components Inc

See all devices from Medical Components Inc →

Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No