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TRANSFORM Occlusion Ballon Catheter - Indonesia BPOM Medical Device Registration

TRANSFORM Occlusion Ballon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003127790. The device is manufactured by STRYKER NEUROVASCULAR from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is WICAKSANA OVERSEAS INTERNATIONAL.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
TRANSFORM Occlusion Ballon Catheter
Analysis ID: AKL 31003127790

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Ireland

Authorized Representative

WICAKSANA OVERSEAS INTERNATIONAL

AR Address

Jl. Ancol Barat VII Blok A5/D No. 2 RT 006 RW 001

Registration Date

Mar 01, 2022

Expiry Date

Jan 31, 2024

Product Type

Therapeutic Neurology Equipment

Intravascular occluding catheter.

Non Electromedic Sterile

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