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Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur) - Albania Medical Device Registration

Access comprehensive regulatory information for Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur) in the Albania medical device market through Pure Global AI's free database. This IIb medical device is manufactured by Boston Scientific Corporation 300 Boston Scientific Way Marlborough, MA 01752 USA. The device was registered on May 10, 2022.

This page provides complete registration details including product model (Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur)), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.

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Albania Official Data
IIb
Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur)
Albania Medical Device Registration
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Product Information

Pajisje mbyllese me fibra te ndertuara te destinuara pernguar ose reduktuar shpejtesine e rrjedhjes se ghjakut ne enet periofarike.

Device Classification
Risk Class
IIb
Product Model
Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur)
Product Name
Interlock™-35 Fibered IDC™ Occlusion System; Interlock™ Fibered IDC™ Occlusion System; IDC™ Interlocking Detachable Coil (sipas listes bashkengjitur)
Registration Information
Registration Date
May 10, 2022
Analysis ID
11965