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Occlutech Atrial Flow Regulator Procedure Pack (with Pistol Pusher) - ARCSA Registration f6122fbc3acec04ec75eae73669d749a

Access comprehensive regulatory information for Occlutech Atrial Flow Regulator Procedure Pack (with Pistol Pusher) in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID f6122fbc3acec04ec75eae73669d749a and manufactured by OCCLUTECH TIBBI URUNLER SAN. VE TIC. LTD. STI. The device was registered on August 22, 2023.

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
f6122fbc3acec04ec75eae73669d749a
Occlutech Atrial Flow Regulator Procedure Pack (with Pistol Pusher)
ARCSA ID: f6122fbc3acec04ec75eae73669d749a
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
OCCLUTECH
Commercial Name
Occluders, Vascular
Registration Information
Analysis ID
f6122fbc3acec04ec75eae73669d749a
Registration Date
August 22, 2023
Expiration Date
August 22, 2028
Product Use

OCCLUTECH AFR IS A PERMANENT CARDIAC IMPLANT INTENDED TO PROTECT AND SECURE THE OUTCOME OF AN ATRIAL BALLOON SEPTOSTOMY.

Manufacturer
Country
TURKEY
Address
YESILKOY SB MAH., E BLOK SOK., OCCLUTECH APT. NO:6, 34149, BAKIRKOY/ ISTANBUL, TURKEY.
Product Owner
Name
OCCLUTECH INTERNATIONAL AB
Country
SWEDEN
Authorized Representative
Address
AV ORELLANA ESQ E9-195 AND AV DECEMBER 6
Phone
22563540