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TENOR STEERABLE GUIDEWIRE - ARCSA Registration e21ac3baa1c7a11a434bdbbc6d0f8bd7

Access comprehensive regulatory information for TENOR STEERABLE GUIDEWIRE in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID e21ac3baa1c7a11a434bdbbc6d0f8bd7 and manufactured by BIOSPHERE MEDICAL SA. The device was registered on February 21, 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
II
e21ac3baa1c7a11a434bdbbc6d0f8bd7
TENOR STEERABLE GUIDEWIRE
ARCSA ID: e21ac3baa1c7a11a434bdbbc6d0f8bd7
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Device Classification
Risk Class
II
Product Type
Invasive
Brand Name
MERIT MEDICAL
Commercial Name
CABLE
Registration Information
Analysis ID
e21ac3baa1c7a11a434bdbbc6d0f8bd7
Registration Date
February 21, 2020
Expiration Date
February 21, 2025
Product Use

THE TENOR STEERABLE GUIDEWIRE IS INTENDED TO FACILITATE THE PLACEMENT OF CATHETERS WITHIN THE PERIPHERAL VASCULATURE FOR VARIOUS DIAGNOSTIC AND INTERVENTIONAL PROCEDURES.

Manufacturer
City
ROISSY IN FRANCE
Country
FRENCH
Address
PARC DES NATIONS PARIS NORD 2 383 RUE DE LA BELLE ETOILE, 95700 ROISSY EN FRANCE
Product Owner
Name
BIOSPHERE MEDICAL SA
Country
FRENCH
Authorized Representative
Address
CALLE BY. LEOPOLDO BENTEZ. INTERSECCIN: OF. JOAQUN ORRANTIA.
Phone
42109097