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VANAV RAY - Indonesia BPOM Medical Device Registration

VANAV RAY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001028323. The device is manufactured by DOCTORS TECH., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MERDIS INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : B
VANAV RAY
Analysis ID: AKL 21001028323

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DOCTORS TECH., LTD

Country of Origin

Korea

Authorized Representative

MERDIS INTERNATIONAL

AR Address

Gedung DBS Bank Tower Lt.12, Unit 1202 A. Ciputra World 1 Jl. Prof. Dr. Satrio Kav.3-5, Karet Kuningan, Setiabudi, Jakarta Selatan

Registration Date

Mar 16, 2023

Expiry Date

Jun 17, 2027

Product Type

Diagnostic Neurology Equipment

Galvanic skin response measurement device.

Non Radiation Electromedics

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