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Roovjoy R-C101I

by Shenzhen roundwhale technology co. LTD.

Roovjoy R-C101I is a Class II device made by Shenzhen roundwhale technology co. LTD., listed in FDA GUDID since 3 Jun 2021 (UDI-DI 00840001700215), 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 Number00840001700215 UDI-DI Date3 Jun 2021ListedStatusListed 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  • Withdrawn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
Roovjoy
Generic name
Transcutaneous electrical stimulation probe
Model / reference
R-C101I
Primary DI / UDI-DI
00840001700215
FDA product code
NGX, IPF, GZJ, NUH
GMDN term
Transcutaneous electrical stimulation probe
Device class
Class II
Regulation number
890.5850, 882.5890
GUDID distribution status
In Commercial Distribution

Related devices

Category: Transcutaneous electrical stimulation electrode, single-usePhysical therapy transcutaneous neuromuscular electrical stimulation systemTranscutaneous electrical stimulation probe

Other devices from Shenzhen roundwhale technology co. LTD.

See all devices from Shenzhen roundwhale technology co. LTD. →

Properties

  • Prescription use
  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)