Skip to content

Lens Holder

by PeriVision SA

Ref LH001

Lens Holder (LH001) is a Class I device made by PeriVision SA, registered in EUDAMED on 8 Jun 2026 (Basic UDI-DI 7649990085LH001F9), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7649990085LH001F9 Basic UDI-DI 07649990085081UDI-DIDate8 Jun 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  • Withdrawn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

Device name
Lens Holder
Model / reference
LH001
Primary DI / UDI-DI
07649990085081
Basic UDI-DI
7649990085LH001F9
EMDN code
Q0299 Ophthalmic devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000047664
Authorised representative
International Associates Auditing & Certification Limited IE-AR-000002248

Similar devices in this category

Other devices filed under OPHTHALMIC DEVICES - OTHER.

Other devices from PeriVision SA

Properties

Other properties (14, all answered No)