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Cardiovascular Procedure Kit 78376

by Terumo Cardiovascular Systems Corporation

Cardiovascular Procedure Kit 78376 is a device made by Terumo Cardiovascular Systems Corporation, listed in FDA GUDID since 23 Oct 2024 (UDI-DI 00699753533103), 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 Number00699753533103 UDI-DI Date23 Oct 2024ListedStatusListed 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  • Withdrawn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
Cardiovascular Procedure Kit
Generic name
Cardiopulmonary bypass system blood tubing set
Model / reference
78376
Primary DI / UDI-DI
00699753533103
GMDN term
Cardiopulmonary bypass system blood tubing set
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiopulmonary bypass system blood tubing set

Other devices from Terumo Cardiovascular Systems Corporation

See all devices from Terumo Cardiovascular Systems Corporation →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)