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I-Asv C1

by Hamilton Medical AG

Ref 161097

Active European Union

CE MDR

Valid until

13 Apr 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV Rheinland LGA Products GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number76300028PN16109739 Basic UDI-DI 07630002813143UDI-DIDate2 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
161097
Primary DI / UDI-DI
07630002813143
Basic UDI-DI
76300028PN16109739
EMDN Code
Z1203010592 Pulmonary ventilators for hospital use - medical device software
Device Class
Class III
Special Device Type
Software
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CH-MF-000013790
Authorised representative
medin Medical Innovations GmbH DE-AR-000006976

Other devices from Hamilton Medical, Inc.

See all devices from Hamilton Medical, Inc. →

Properties

Other properties (13)

  • 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