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i-Stitch up

by A.M.I. Agency for Medical Innovations GmbH United States EUDAMED

Ref IST1040

EMDN A018002

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EAMIA3B9C1D1KW Basic UDI-DIDate23 Jun 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
i-Stitch Instruments
Model / Reference
IST1040
Primary DI / UDI-DI
+EAMIIST10400
Basic UDI-DI
++EAMIA3B9C1D1KW
Direct Marketing DI
+EAMIIST10400
EMDN Code
A018002 Needle guides
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
AT-MF-000016792

Other devices from A.M.I. Agency for Medical Innovations GmbH

See all devices from A.M.I. Agency for Medical Innovations GmbH →

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 eb093c43-0287-4794-90b0-67da02c1de57 61 fields · synced 24 Oct 2026