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Inüo Blunt Tip

by Termosalud, S.L.

Ref AR00010662Model INÜO BLUNT TIP

Inüo Blunt Tip (AR00010662) is a Class I device made by Termosalud, S.L., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 843660129IBTIPE7), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843660129IBTIPE7 Basic UDI-DI 08436601290311UDI-DIDate30 Oct 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
INÜO BLUNT TIP, AR00010662
Primary DI / UDI-DI
08436601290311
Basic UDI-DI
843660129IBTIPE7
EMDN code
Z12040280 General medicine therapeutic treatment instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000019177

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See all devices from Termosalud, S.L. →

Properties

Other properties (14, all answered No)