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Nupro 90741L03

by Dentsply Professional

Nupro 90741L03 is a Class II device made by Dentsply Professional, listed in FDA GUDID since 31 Jan 2017 (UDI-DI D00390741L031), 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 NumberD00390741L031 UDI-DI Date31 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  • Withdrawn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
Nupro
Generic name
Cable/lead/sensor/probe cover, non-sterile
Model / reference
90741L03
Primary DI / UDI-DI
D00390741L031
FDA product code
PEM, EKX
GMDN term
Cable/lead/sensor/probe cover, non-sterile
Device class
Class II
Regulation number
878.4370, 872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental polishing cup, single-useCable/lead/sensor/probe cover, non-sterile

Other devices from Dentsply Professional

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Properties

  • Sterilise before use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)