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ARGOS Biometer - Indonesia BPOM Medical Device Registration

ARGOS Biometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420195. The device is manufactured by SANTEC OIS CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BINASUKSES CANTEEN.

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
ARGOS Biometer
Analysis ID: AKL 21201420195

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. BINASUKSES CANTEEN

AR Address

Jl. Pulo Kambing II No. 26 Kawasan Industri Pulogadung, Kel. Jatinegara, Kec. Cakung, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos 13930

Registration Date

Oct 30, 2024

Expiry Date

Mar 21, 2027

Product Type

Diagnostic Eye Equipment

Optical Coherence Tomography

Non Radiation Electromedics

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