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PlanPoint Software

by Intuitive Surgical, Inc.

Ref 610210

PlanPoint Software (610210) is a Class IIa device made by Intuitive Surgical, Inc., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 08868741230107E), 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 Number08868741230107E Basic UDI-DI 00886874123713UDI-DIDate5 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
610210
Primary DI / UDI-DI
00886874123713
Basic UDI-DI
08868741230107E
EMDN code
Z12020892 Pulmonary endoscopic instruments - medical device software
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000020711
Authorised representative
Intuitive Surgical SAS FR-AR-000009053

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Properties

Other properties (14, all answered No)