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Meritrans DTXPlus® 10884450323240

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 Number10884450323240 UDI-DI Date3 Apr 2019ListedStatusListed 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  • Withdrawn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 blood pressure transducer set
Model / Ref / Catalog
10884450323240, 682147/A
Primary DI / UDI-DI
10884450323240
FDA Product Code
DXN
GMDN Term
Invasive blood pressure transducer set
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Invasive blood pressure transducer set

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

See all devices from Argon Critical Care Systems Singapore Pte. Ltd. →

Properties

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

Other properties (10)

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