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HOCOMA Andago V2.0 - Indonesia BPOM Medical Device Registration

HOCOMA Andago V2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403420300. The device is manufactured by HOCOMA AT from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. AIRINDO MEDIKA CENTER.

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BPOM Registered
Risk Class Kelas Resiko : A
HOCOMA Andago V2.0
Analysis ID: AKL 11403420300

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HOCOMA AT

Country of Origin

Switzerland

Authorized Representative

PT. AIRINDO MEDIKA CENTER

AR Address

Jalan Teuku Nyak Arief NO. 10

Registration Date

Aug 01, 2024

Expiry Date

Aug 01, 2029

Product Type

Therapeutic Physical Health Equipment

Powered exercise equipment.

Non Radiation Electromedics

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