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Cannula Insertion System

by Medical Instrument Development Laboratories, Inc. 2 variants

Ref 5700

Cannula Insertion System (5700) is a medical device (EU MDD Class IIa; EMDN category ophthalmic surgery instruments) made by Medical Instrument Development Laboratories, Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-10812480013718), 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-10812480013718 Basic UDI-DI 10812480013718UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
5700
Primary DI / UDI-DI
10812480013718
Basic UDI-DI
B-10812480013718
EMDN code
Q021199 Ophthalmic surgery instruments, single-use - other
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000033104
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Similar devices in this category

Other devices filed under OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Medical Instrument Development Laboratories, Inc.

See all devices from Medical Instrument Development Laboratories, Inc. →

Properties

  • Supplied sterile
Other properties (11, all answered No)