Specify® SureScan® MRI 2x8 lead kits - ARCSA Registration a5d4c6de4c6b35718f7dc0ad59a55bb8
Access comprehensive regulatory information for Specify® SureScan® MRI 2x8 lead kits in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID a5d4c6de4c6b35718f7dc0ad59a55bb8 and manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA. The device was registered on March 15, 2018.
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
IV
a5d4c6de4c6b35718f7dc0ad59a55bb8
Specify® SureScan® MRI 2x8 lead kits
ARCSA ID: a5d4c6de4c6b35718f7dc0ad59a55bb8
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
MEDTRONIC
Commercial Name
Electrodes, for Neuromuscular Stimulators
Sterilization Method
ETHYLENE OXIDE
Registration Information
Analysis ID
a5d4c6de4c6b35718f7dc0ad59a55bb8
Registration Date
March 15, 2018
Expiration Date
March 15, 2023
Creation Date
March 15, 2018
Product Use
THEY ARE PART OF A NEUROSTIMULATION SYSTEM FOR PAIN THERAPY
Manufacturer
City
VILLALBA
Country
PUERTO RICO
Address
RD. 149, KM. 56.3CALL BOX 6001VILLALBA, PR 00766
Product Owner
Name
MEDTRONIC INC
Country
UNITED STATES
Authorized Representative
Address
AV. 23 RODRIGO DE CHAVEZ S/N CIUDAD COLON MZ.274-EDF. BUSINESS 2 OFFICE 308.
Phone
3901954