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SPOON EXPLORER - EUDAMED Registration D123103370

Access comprehensive regulatory information for SPOON EXPLORER 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 D123103370 and manufactured by Dental Expert in Pakistan.

This page provides complete registration details including trade name (SPOON EXPLORER), manufacturer information, authorized representative details, competent authority (DE/CA38 - Regierungspräsidium Karlsruhe), 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.

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EUDAMED Official Data
Class I
D123103370
No
SPOON EXPLORER
Trade Name: SPOON EXPLORER
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Device Description (EMDN)

DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE

Device Classification
Risk Class
Class I
CND Nomenclatures Code
L159003
Trade Name
SPOON EXPLORER
Implantable
No
Reusable
Yes
Measuring Function
No
Registration Information
Primary DI
D123103370
Basic UDI
++D12310337BW
Version Date
August 06, 2024
Manufacturer Last Update
June 01, 2022
Active Status
No
Manufacturer
Manufacturer Name
Dental Expert
Country
Pakistan
Country Type
NON_EU
Address
237-A Street No.18, MAG TOWN, SIALKOT, PAKISTAN 51310 Sialkot
Email
azambhatti71@gmail.com
Authorized Representative
SRN
DE-AR-000008078
Country
Germany
Address
6 Hans Bunte Strasse Heidelberg
Email
info@antex-medi-solution.de
Telephone
+4915678612574
Regulatory Information
Competent Authority
DE/CA38 - Regierungspräsidium Karlsruhe
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Italy
Device Characteristics
Human Tissues
No
Animal Tissues
No