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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 21003420014. 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 INTER-SON PARTNERS.

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BPOM Registered
Risk Class Kelas Resiko : C
JUMPER ™ TENS THERAPY DEVICE
Analysis ID: AKL 21003420014

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

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

Feb 19, 2024

Expiry Date

Nov 24, 2028

Product Type

Therapeutic Neurology Equipment

Transcutaneous electrical nerve stimulator for pain relief.

Non Radiation Electromedics

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