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Surge Cardiovascular PER-3003

by Med Michigan Holdings LLC

Surge Cardiovascular PER-3003 is a cardioplegia solution administration adaptor (FDA Class II; FDA product code DWF, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass) made by Med Michigan Holdings LLC, listed in FDA GUDID since 26 Mar 2018 (UDI-DI 00817278011122), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817278011122 UDI-DI Date26 Mar 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Surge Cardiovascular
Generic name
Cardioplegia solution administration adaptor
Model / Ref / Catalog
PER-3003
Primary DI / UDI-DI
00817278011122
FDA product code
DWF
GMDN term
Cardioplegia solution administration adaptor
Device class
Class II
Regulation number
870.4210
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Cardioplegia solution administration adaptor

Similar devices

Other devices filed under FDA product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass).

Other devices from Med Michigan Holdings LLC

See all devices from Med Michigan Holdings LLC →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)