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Pro-Ject Injector system

by Bio-Tech Vision Care Pvt. Ltd. India EUDAMED

Ref Pro-Ject ScrewModel Pro-Ject Push

EMDN L1709

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8905286PRO-JECTEM Basic UDI-DIDate2 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Pro-Ject Injector system
Model / Reference
Pro-Ject Push, Pro-Ject Screw
Primary DI / UDI-DI
08905286869162
Basic UDI-DI
8905286PRO-JECTEM
EMDN Code
L1709 Ocular implant instruments not included in other classes, reusable
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
IN-MF-000008482
Authorised representative
Biotech Europe Meditech Inc Limited IE-AR-000004696

Other devices from Bio-Tech Vision Care Pvt. Ltd.

See all devices from Bio-Tech Vision Care Pvt. Ltd. →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
Other properties (12)
  • Sterile: No
  • Implantable: 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

Sources (1)

  • EUDAMED 243eebde-a388-4c90-8b3b-ad1aeaaf9500 61 fields · synced 24 Oct 2026