08435566614200

Titanium screws

IMPLANT PROTESIS DENTAL 2004 S.L.·Class IIb·EU EUDAMED·Trade name: Ti Screw Ø 5,5No
Device classification
Risk class
Class IIb
CND nomenclatures code
Q010280
Trade name
Ti Screw Ø 5,5
Implantable
Yes
Reusable
No
Measuring function
No
Registration information
Primary DI
08435566614200
Basic UDI
8435566610BM
Active status
No
Manufacturer
Country
Spain
Country type
EU_MEMBER_STATE
Address
9-15 Rosa dels Vents Premià de Dalt
Email
despinach@ipd2004.com
Regulatory information
Competent authority
Agencia Española de Medicamentos y Productos Sanitarios
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Spain
Market available
Belgium:2024-10-22~None, Bulgaria:2024-09-16~None, Croatia:2024-10-22~None, Cyprus:2024-09-16~None, Czechia:2024-10-22~None, Denmark:2024-10-22~None, France:2024-10-22~None, Germany:2024-10-22~None, Greece:2024-10-22~None, Hungary:2024-10-22~None, Ireland:2024-10-22~None, Italy:2024-10-22~None, Lithuania:2024-10-22~None, Luxembourg:2024-10-22~None, Netherlands:2024-10-22~None, Poland:2024-10-22~None, Portugal:2024-10-22~None, Romania:2024-10-22~None, Slovakia:2024-10-22~None, Spain:2024-10-22~None, Sweden:2024-10-22~None, United Kingdom (Northern Ireland only):2024-10-22~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

PROSTHETIC DENTISTRY DEVICES - ACCESSORIES

About this record

Access comprehensive regulatory information for Titanium screws in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 08435566614200 and manufactured by IMPLANT PROTESIS DENTAL 2004 S.L. in Spain.

This page provides complete registration details including trade name (Ti Screw Ø 5,5), manufacturer information, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.