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INTICA 7 HF-T - Indonesia BPOM Medical Device Registration

INTICA 7 HF-T is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503910634. The device is manufactured by BIOTRONIK SE & CO., KG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRANSMEDIC 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 : D
INTICA 7 HF-T
Analysis ID: AKL 30503910634

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

Perkantoran Menara Era Unit G-01 & G-02 Jl. Senen Raya No 135-137, Kel. Senen Kec. Senen, Jakarta Pusat 10410

Registration Date

Feb 21, 2019

Expiry Date

Dec 31, 2023

Product Type

Prosthetic Cardiology Equipment

Automatic Implantable Cardioverter Defibrillator With Cardiac Resynchronization (Crt-D)

Non Radiation Electromedics

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