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EUDAMED registration 08800171201433No

Gutta Percha Points #140

ACEONEDENT KOREA INDUSTRIAL CO.Class IIaEU EUDAMEDTrade name: ACEONEDENT KOREA IND. CO.
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
Q01010299
Trade name
ACEONEDENT KOREA IND. CO.
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
08800171201433
Basic UDI
B-08800171201433
Version date
January 16, 2025
Manufacturer last update
March 21, 2024
Active status
No
Manufacturer
Manufacturer name
ACEONEDENT KOREA INDUSTRIAL CO.
Country
Republic of Korea
Country type
NON_EU
Address
22 Samjak - ro Bucheon-si
Email
aceonedent@hanmail.net
Authorized representative
Name
JaviTech e.K.
SRN
DE-AR-000005875
Country
Germany
Address
16 Sachsenhausener Straße Schwalbach am Taunus
Email
info@javitech.de
Telephone
+49 6196 4021549
Regulatory information
Competent authority
DE/CA29 - Regierungspräsidium Darmstadt Abteilung Arbeitsschutz und Umwelt
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
Germany
Market available
Germany:None~None, Greece:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

ROOT CANAL FILLING DEVICES - OTHER

About this record

Access comprehensive regulatory information for Gutta Percha Points #140 in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 08800171201433 and manufactured by ACEONEDENT KOREA INDUSTRIAL CO. in Republic of Korea.

This page provides complete registration details including trade name (ACEONEDENT KOREA IND. CO.), manufacturer information, authorized representative details, competent authority (DE/CA29 - Regierungspräsidium Darmstadt Abteilung Arbeitsschutz und Umwelt), 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.