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PIEZOWAVE Extracorporeal Shockwave Therapy - Indonesia BPOM Medical Device Registration

PIEZOWAVE Extracorporeal Shockwave Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31403220371. The device is manufactured by RICHARD WOLF GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is SURGIKA ALKESINDO.

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Risk Class Kelas Resiko : D
PIEZOWAVE Extracorporeal Shockwave Therapy
Analysis ID: AKL 31403220371

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

RICHARD WOLF GMBH.

Country of Origin

Germany

Authorized Representative

SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Dec 08, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Physical Health Equipment

Extracorporeal shock wave treatment device

Non Radiation Electromedics

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