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Rinn® 550200

by Dentsply International

Rinn® 550200 is a Class II device made by Dentsply International, listed in FDA GUDID since 27 Jan 2017 (UDI-DI D0035502001), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD0035502001 UDI-DI Date27 Jan 2017ListedStatusListed 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  • Withdrawn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
Rinn®
Generic name
Cable/lead/sensor/probe cover, non-sterile
Model / reference
550200
Primary DI / UDI-DI
D0035502001
FDA product code
PEM
GMDN term
Cable/lead/sensor/probe cover, non-sterile
Device class
Class II
Regulation number
878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cable/lead/sensor/probe cover, non-sterile

Other devices from Dentsply International

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)