Endo-M. Modular KneeProsth.,Fem.Segment,Tilastan®, lateral,L1, H=20 mm, right - ARCSA Registration feb3e40de860da396f19fbeeb26fcc4d
Access comprehensive regulatory information for Endo-M. Modular KneeProsth.,Fem.Segment,Tilastan®, lateral,L1, H=20 mm, right in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID feb3e40de860da396f19fbeeb26fcc4d and manufactured by WALDEMAR LINK GMBH Y CO. KG. The device was registered on February 05, 2015.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
III
feb3e40de860da396f19fbeeb26fcc4d
Endo-M. Modular KneeProsth.,Fem.Segment,Tilastan®, lateral,L1, H=20 mm, right
ARCSA ID: feb3e40de860da396f19fbeeb26fcc4d
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
Endo-Model
Commercial Name
Prosthesis, Joint, for knee, total
Sterilization Method
GAMMA IRRADIATION
Registration Information
Analysis ID
feb3e40de860da396f19fbeeb26fcc4d
Registration Date
February 05, 2015
Expiration Date
February 05, 2025
Creation Date
February 22, 2021
Product Use
KNEE JOINT REPLACEMENT
Manufacturer
Product Owner
Name
WALDEMAR LINK GMBH Y CO. KG
Country
GERMANY
Authorized Representative
Address
AV. 12 DE OCTUBRE N24-739 Y AV COLON TORRE BOREAL PISO 1 OF 103
Phone
23945303