Skip to content

ANF Therapy® M2

by Amino Frequency Corporation Sl.

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 Number08436587170843 UDI-DI Date15 May 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  • Withdrawn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
ANF Therapy®
Generic Name
Physical therapy insulation patch
Model / Reference
M2
Primary DI / UDI-DI
08436587170843
FDA Product Code
IMD
GMDN Term
Physical therapy insulation patch
Device Class
Class I
Regulation Number
890.5710
GUDID distribution status
In Commercial Distribution

Other devices from Amino Frequency Corporation Sl.

See all devices from Amino Frequency Corporation Sl. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No