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Dentapen Battery Dentapen for Dentapen

by Juvaplus SA

Dentapen Battery Dentapen for Dentapen (BP04) is a Class II device made by Juvaplus SA, listed in FDA GUDID since 22 Oct 2018 (UDI-DI EJUVBP047), 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 NumberEJUVBP047 UDI-DI Date22 Oct 2018ListedStatusListed 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  • Withdrawn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
Dentapen Battery
Generic name
Dental anaesthesia syringe, reusable
Model / Ref / Catalog
Dentapen for Dentapen, BP04
Primary DI / UDI-DI
EJUVBP047
FDA product code
EJI
GMDN term
Dental anaesthesia syringe, reusable
Device class
Class II
Regulation number
872.6770
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EJI (Syringe, Cartridge).

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Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)