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Centurion CWHG001-5

by Centurion Medical Products

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 Number10653160306603 UDI-DI Date30 Mar 2017ListedStatusListed 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  • Withdrawn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
Centurion
Generic Name
Invasive-pressure external transducer, single-use
Model / Reference
CWHG001-5
Primary DI / UDI-DI
10653160306603
FDA Product Code
DRS
GMDN Term
Invasive-pressure external transducer, single-use
Device Class
Class II
Regulation Number
870.2850
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Invasive-pressure external transducer, single-use

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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