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G5® Me 600

by General Physiotherapy Inc

G5 Me 600 is a hand-held electric massager (FDA Class I; FDA product code ISA, Massager, Therapeutic, Electric) made by General Physiotherapy Inc, listed in FDA GUDID since 12 Jun 2017 (UDI-DI 00746980002190), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00746980002190 UDI-DI Date12 Jun 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
G5®
Generic name
Hand-held electric massager
Model / Ref / Catalog
ME 600
Primary DI / UDI-DI
00746980002190
FDA product code
ISA
GMDN term
Hand-held electric massager
Device class
Class I
Regulation number
890.5660
GUDID distribution status
In Commercial Distribution
Size
Weight — 8 Pound

Related devices

Category: Hand-held electric massager

Other devices from General Physiotherapy Inc

See all devices from General Physiotherapy Inc →

Properties

  • Convenience kit
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)