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Abdominal Aortic Junctional Tourniquet – Stabilised (AAJT-S)

by Compression Works, Inc

Ref AAJT-S001

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00860002227504 UDI-DI Date20 Mar 2023ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number008600002227504VY Basic UDI-DI 00860002227504UDI-DIDate7 Mar 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Abdominal Aortic Junctional Tourniquet – Stabilised (AAJT-S) EUDAMED
Abdominal Aortic & Junctional Tourniquet (Stabilized) - AAJT-S GUDID
Generic Name
Emergency junctional haemorrhage compression set
Model / Reference
AAJT-S001
Primary DI / UDI-DI
00860002227504
Basic UDI-DI
008600002227504VY
510(k) Number
FDA Product Code
DXC
EMDN Code
C90010301 Haemostasis mechanical systems (including single-use tourniquets)
GMDN Term
Emergency junctional haemorrhage compression set
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
870.4450
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000021119
Authorised representative
Elara Pharmaservices Europe Ltd IE-AR-000011852

Other devices from Compression Works, Inc

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No