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Monoplace Hyperbaric Chambers 32” to 40"

by TEKNA Manufacturing Pvt Ltd 2 variants

Ref Hybrid 3200/32

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-08906124940036 Basic UDI-DI 08906124940036UDI-DIDate1 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Hybrid 3200/32
Primary DI / UDI-DI
08906124940036
Basic UDI-DI
B-08906124940036
EMDN Code
Z120308 Hyperbaric chambers
Device Class
Class IIb
Special Device Type
-1192
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IN-MF-000020411
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Tekna Manufacturing Pvt. Ltd.

Properties

  • Administering Medicine

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No