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Mako

by MAKO Surgical Corp. 4 variants

Ref 700002606012Model 08858251002237SK

Mako (700002606012) is a Class I device made by MAKO Surgical Corp., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 08858251002237SK), 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 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/MDR Number08858251002237SK Basic UDI-DI 07613327625561UDI-DIDate26 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
TD-01 - MAKO - Class I - Clinical Trays and Bowles - Metal and Plastic
Model / reference
08858251002237SK, 700002606012
Primary DI / UDI-DI
07613327625561
Basic UDI-DI
08858251002237SK
Direct marketing DI
07613327625561
EMDN code
V0402 Clinical use trays and bowls
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000000703
Authorised representative
Stryker European Operations Limited IE-AR-000000092

Other devices from MAKO Surgical Corp.

See all devices from MAKO Surgical Corp. →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)