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Cellec V - Indonesia BPOM Medical Device Registration

Cellec V is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403120077. The device is manufactured by JEISYS MEDICAL INC from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is REGENESIS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
Cellec V
Analysis ID: AKL 21403120077

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

JEISYS MEDICAL INC

Country of Origin

Korea

Authorized Representative

REGENESIS INDONESIA

AR Address

Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan

Registration Date

Jan 07, 2021

Expiry Date

Sep 21, 2025

Product Type

Therapeutic Physical Health Equipment

Microwave diathermy.

Non Radiation Electromedics

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