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INTRADYN Tear Away Introducers - Indonesia BPOM Medical Device Registration

INTRADYN Tear Away Introducers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501715045. The device is manufactured by AESCULAP CHIFA SP. Z.O.O. from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. B. BRAUN MEDICAL INDONESIA.

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 : B
INTRADYN Tear Away Introducers
Analysis ID: AKL 20501715045

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Poland

Authorized Representative

PT. B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Apr 12, 2021

Expiry Date

Aug 03, 2025

Product Type

Diagnostic Cardiology Equipment

Catheter introducer.

Non Electromedic Sterile

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