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Ily

by Sterlab 51 variants

Ref 2003AModel 2003

Ily (2003A) is a Class I device made by Sterlab, registered in EUDAMED on 28 Jan 2026 (Basic UDI-DI 376031457MANETTEJB), 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 Number376031457MANETTEJB Basic UDI-DI 03760314570046UDI-DIDate28 Jan 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  • Withdrawn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
Manette Ily
Model / reference
2003, 2003A
Primary DI / UDI-DI
03760314570046
Basic UDI-DI
376031457MANETTEJB
Direct marketing DI
03760314570046
EMDN code
Z12020101 Robot-assisted endoscopic surgery systems
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
FR-MF-000001369

Similar devices in this category

Other devices filed under ROBOT-ASSISTED ENDOSCOPIC SURGERY SYSTEMS.

Other devices from Sterlab

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Properties

Other properties (14, all answered No)