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Riptide Aspiration Pump

by Micro Therapeutics Inc, d/b/a Ev3 Neurovascular

Ref MAP-1000EU

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763000B00010757L Basic UDI-DI 00763000300678UDI-DIDate6 Nov 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Riptide Aspiration Pump
Model / Reference
MAP-1000EU
Primary DI / UDI-DI
00763000300678
Basic UDI-DI
0763000B00010757L
EMDN Code
C010402020702 Mechanical peripheral thrombectomy and thromboaspiration systems
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000019796
Authorised representative
Medtronic B.V. NL-AR-000006050

Other devices from Micro Therapeutics, Inc. d/b/a ev3 Neurovascular

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Properties

  • Reusable
  • Contains Latex

Other properties (11)

  • Sterile: No
  • Implantable: 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