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VEINOPLUS Arterial - Indonesia BPOM Medical Device Registration

VEINOPLUS Arterial is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403819209. The device is manufactured by AD REM TECHNOLOGY. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDONESIA GLOBAL MEDIKA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
VEINOPLUS Arterial
Analysis ID: AKL 21403819209

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AD REM TECHNOLOGY.

Country of Origin

France

Authorized Representative

INDONESIA GLOBAL MEDIKA

AR Address

APL Tower 16th floor, T9 Podomoro City, (Central Park) Jl. LetJend S. Parman Kav 28, Jakarta 11470 INDONESIA

Registration Date

Nov 22, 2022

Expiry Date

Jul 05, 2027

Product Type

Therapeutic Physical Health Equipment

Powered muscle stimulator.

Non Radiation Electromedics

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