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JUMPER ™ TENS Therapy Device - Indonesia BPOM Medical Device Registration

JUMPER ™ TENS Therapy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003915090. The device is manufactured by SHENZHEN JUMPER MEDICAL EQUIPMENT CO,. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INTER-SON PARTNERS.

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BPOM Registered
Risk Class Kelas Resiko : C
JUMPER ™ TENS Therapy Device
Analysis ID: AKL 21003915090

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTER-SON PARTNERS

AR Address

MTH SQUARE LT.DASAR NO.A8A-A8B JL. MT HARYONO KAV.10 BIDARA CINA JATINEGARA - JAKARTA TIMUR 13330

Registration Date

Aug 12, 2019

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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