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Apollo TMS Pro 919001

by MAG & More GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04260526050118 UDI-DI Date9 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Apollo TMS Pro
Generic Name
Magnetic neural stimulation system
Model / Reference
919001
Primary DI / UDI-DI
04260526050118
FDA Product Code
OBP, QCI
GMDN Term
Magnetic neural stimulation system
Device Class
Class II
Regulation Number
882.5805, 882.5802
GUDID distribution status
In Commercial Distribution

Other devices from MAG & More GmbH

See all devices from MAG & More GmbH →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

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