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MASTERPULS ONE - Indonesia BPOM Medical Device Registration

MASTERPULS ONE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320511. The device is manufactured by STORZ MEDICAL AG from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INNOMED JAYA UTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
MASTERPULS ONE
Analysis ID: AKL 21403320511

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

STORZ MEDICAL AG

Country of Origin

Switzerland

Authorized Representative

INNOMED JAYA UTAMA

AR Address

Jl. Cideng Barat No.64 #02-01, Cideng Barat nomor 64 #02-01, Kel. Cideng, Kec. Gambir, Jakarta Pusat, DKI Jakarta

Registration Date

Apr 19, 2023

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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