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SmartVap™

by Technologie Institut Medizin GmbH (TIM) 11 variants

Ref SV-S-P

SmartVap (SV-S-P) is a medical device (EU MDD Class IIb; EMDN category respiratory and anaesthesia devices) made by Technologie Institut Medizin GmbH (TIM), registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04260665920754), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260665920754 Basic UDI-DI 04260665920754UDI-DIDate5 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
SmartVap
Model / reference
SV-S-P
Primary DI / UDI-DI
04260665920754
Basic UDI-DI
B-04260665920754
EMDN code
R9099 Respiratory and anaesthesia devices - other
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000018722

Similar devices in this category

Other devices filed under RESPIRATORY AND ANAESTHESIA DEVICES - OTHER.

Other devices from Technologie Institut Medizin GmbH (TIM)

See all devices from Technologie Institut Medizin GmbH (TIM) →

Properties

  • Administering medicine
Other properties (11, all answered No)