Herbert Screw Cannulated - ARCSA Registration f891eea37b936c3a33c6e61bbf4c10d6
Access comprehensive regulatory information for Herbert Screw Cannulated in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID f891eea37b936c3a33c6e61bbf4c10d6 and manufactured by APOTHECARIES SUNDRIES MANUFACTURING CO.. The device was registered on October 16, 2020.
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
f891eea37b936c3a33c6e61bbf4c10d6
Herbert Screw Cannulated
ARCSA ID: f891eea37b936c3a33c6e61bbf4c10d6
Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
DISGUST
Commercial Name
Orthopedic External Fixation Systems for Fractures
Registration Information
Analysis ID
f891eea37b936c3a33c6e61bbf4c10d6
Registration Date
October 16, 2020
Expiration Date
October 16, 2025
Product Use
SCREWS ARE SURGICAL IMPLANTS THAT ARE PART OF THE INTERNAL FIXATION SYSTEM FOR FRACTURES
Manufacturer
City
NEW DELHI
Country
INDIA
Address
ASCO HOUSE 13, COMMUNITY CENTRE MAYAPURI, PHASE I NEW DELHI 110 064 INDIA
Product Owner
Name
APOTHECARIES SUNDRIES MANUFACTURING CO.
Country
INDIA
Authorized Representative
Address
CITADEL: LA MARISCAL STREET: RAMIREZ DAVALOS N° E3-10
Phone
59322545525