Pure Global

OCCLUTECH Guide Wire - Indonesia BPOM Medical Device Registration

OCCLUTECH Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501910749. The device is manufactured by EPFLEX FEINWERKTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
OCCLUTECH Guide Wire
Analysis ID: AKL 20501910749

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Sep 16, 2023

Expiry Date

Jan 27, 2028

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing