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RENAMIC - Indonesia BPOM Medical Device Registration

RENAMIC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501811363. The device is manufactured by BIOTRONIC SE & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
RENAMIC
Analysis ID: AKL 20501811363

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Jul 01, 2019

Expiry Date

Mar 31, 2024

Product Type

Diagnostic Cardiology Equipment

Programmable diagnostic computer.

Non Radiation Electromedics

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