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Test - Indonesia BPOM Medical Device Registration

Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11301220009. The device is manufactured by TEST from Bangladesh, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PYRIDAM FARMA.

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 : A
Test
Analysis ID: AKL 11301220009

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TEST

Country of Origin

Bangladesh

Authorized Representative

PYRIDAM FARMA

AR Address

Sinarmas MSIG Tower Lt. 12 Jl. Jenderal Sudirman Kav. 21 Kelurahan Karet

Registration Date

Feb 08, 2022

Expiry Date

Feb 06, 2025

Product Type

Diagnostic Orthopedic Equipment

Nonpowered goniometer.

Electromedic Radiation

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