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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 20501420410. The device is manufactured by BIOTRONIK SE & CO., KG from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DCH AURIGA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
RENAMIC
Analysis ID: AKL 20501420410

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

DCH AURIGA INDONESIA

AR Address

DCH AURIGA INDONESIA

Registration Date

Aug 05, 2024

Expiry Date

Aug 21, 2028

Product Type

Diagnostic Cardiology Equipment

Programmable diagnostic computer.

Non Radiation Electromedics

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