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Axilum Robotics TMS-Cobot adaptation kit for MagVenture Cool-B65-RO SLS coil

by Axilum Robotics

Ref 2-02-02, 2-02-27, 2-02-19, 2-02-08Model TMS-Cobot-2

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number370135462-01-024B Basic UDI-DI Date24 May 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number03701354620223 UDI-DI Date23 Jan 2020ListedStatusListed GUDID: in commercial distribution

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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Axilum Robotics TMS-Cobot adaptation kit for MagVenture Cool-B65-RO SLS coil EUDAMED
Axilum Robotics TMS-Cobot adaptation kit for MagVenture Cool-B65-A/P-CO coil EUDAMED
Axilum Robotics GUDID
Generic Name
Magnetic neural stimulation system
Device Name
Axilum Robotics TMS-Cobot
Model / Ref / Catalog
TMS-Cobot-2, 2-02-02, 2-02-27, 2-02-19, 2-02-08, ADAP-MAGV-CB65AP-11
Primary DI / UDI-DI
03701354620223, 03701354600102, 03701354600119, 03701354620285
Basic UDI-DI
370135462-01-024B
Direct Marketing DI
03701354620223
03701354600102
03701354600119
03701354620285
510(k) Number
FDA Product Code
QFF
EMDN Code
Z12101199 Peripheral or central neuro stimulation and assessment instruments - other
GMDN Term
Magnetic neural stimulation system
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
882.5805
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
TMS-Cobot-2
2-02-02
2-02-27
2-02-19
2-02-08
GUDID
ADAP-MAGV-CB65AP-11
Device ClassEUDAMED
Class IIa
GUDID
Class II

Manufacturer details

EUDAMED SRN
FR-MF-000001731

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Properties

  • Prescription Use
  • Combination Product
  • Serial Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No