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MagPro Accessories Vacum Pillow 70 cm

by Tonica Elektronik A/S

Ref 9016B0132

MagPro Accessories Vacum Pillow 70 cm (9016B0132) is a magnetic neural stimulation system (EU MDR Class I; FDA Class II) made by Tonica Elektronik A/S, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 5713484VacuumPumpUnitLQ) and listed in FDA GUDID since 28 Nov 2022 (UDI-DI 05713484031341), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5713484VacuumPumpUnitLQ Basic UDI-DI 05713484031341UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05713484031341 UDI-DI Date28 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 5713484VacuumPumpUnitLQ registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 05713484031341 listed 28 Nov 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05713484031341
  2. Registered EUDAMED 5713484VacuumPumpUnitLQ

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  • Withdrawn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
Vacuum Pillow 70cm EUDAMED
MagPro Accessories GUDID
Generic name
Magnetic neural stimulation system
Device name
Vacuum Pump Unit
Model / Ref / Catalog
9016B0132, Vacum Pillow 70 cm
Primary DI / UDI-DI
05713484031341
Basic UDI-DI
5713484VacuumPumpUnitLQ
FDA product code
OBP, QCI
EMDN code
Z12101180 Peripheral or central neuro stimulation and assessment instruments - hardware accessories
GMDN term
Magnetic neural stimulation system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.5805, 882.5802
EU registration type
Standard device
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
9016B0132
GUDID
Vacum Pillow 70 cm
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Magnetic neural stimulation system

Similar devices in this category

Other devices filed under PERIPHERAL OR CENTRAL NEURO STIMULATION AND ASSESSMENT INSTRUMENTS.

Other devices from Tonica Elektronik A/S

See all devices from Tonica Elektronik A/S →

Properties

  • Prescription use
  • Manufacturing date
Other properties (23, all answered No)