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CentriMag™ 201-30500

by Thoratec Corporation

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

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 Number07640135140153 UDI-DI Date19 Feb 2026ListedStatusListed GUDID: 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  • Withdrawn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
CentriMag™
Generic Name
Image display unit, colour
Model / Ref / Catalog
201-30500
Primary DI / UDI-DI
07640135140153
FDA Product Code
OJE, DSQ, DWA
GMDN Term
Image display unit, colour
Device Class
Unclassified
Regulation Number
870.4380
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Thoratec Corporation

See all devices from Thoratec Corporation →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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