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Meritrans DTXPlus® 10884450322557

by Argon Critical Care Systems Singapore Pte. Ltd.

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 Number10884450322557 UDI-DI Date26 Jan 2018ListedStatusListed 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  • Withdrawn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
Meritrans DTXPlus®
Generic Name
Invasive-pressure external transducer, single-use
Model / Reference
10884450322557
Primary DI / UDI-DI
10884450322557
FDA Product Code
DXN
GMDN Term
Invasive-pressure external transducer, single-use
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Invasive-pressure external transducer, single-useInvasive blood pressure transducer set

Other devices from Argon Critical Care Systems Singapore Pte. Ltd.

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Properties

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

Other properties (8)

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