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EUDAMED registration 10789594000005No

DPI Micro-Applicators

Young Microbrush LLC dba Microbrush InternationalClass IEU EUDAMEDTrade name: DPI Micro-Applicator M8 Fine Assorted 400 Trays w/Cap
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
Q0199
Trade name
DPI Micro-Applicator M8 Fine Assorted 400 Trays w/Cap
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
10789594000005
Basic UDI
0789594DPIMAM87R
Version date
October 19, 2022
Manufacturer last update
May 08, 2023
Active status
No
Manufacturer
Manufacturer name
Young Microbrush LLC dba Microbrush International
Country
United States
Country type
NON_EU
Address
1376 Cheyenne Ave Grafton
Email
customerservice@younginnovations.com
Authorized representative
Name
Young Microbrush Ireland Ltd
SRN
IE-AR-000011249
Country
Ireland
Address
Clogherane Dungarven, County Waterford
Email
YMBI@younginnovations.com
Telephone
+ 35 3 584 59 66
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Market available
Germany:2021-04-20~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

ODONTOLOGY DEVICES - OTHER

About this record

Access comprehensive regulatory information for DPI Micro-Applicators in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 10789594000005 and manufactured by Young Microbrush LLC dba Microbrush International in United States.

This page provides complete registration details including trade name (DPI Micro-Applicator M8 Fine Assorted 400 Trays w/Cap), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.