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SANYMED BILIRUBIN DIRECT LR - Indonesia BPOM Medical Device Registration

SANYMED BILIRUBIN DIRECT LR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101916021. The device is manufactured by SANYMED S.A.S from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERFECT MEDILAB INDONESIA.

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
SANYMED BILIRUBIN DIRECT LR
Analysis ID: AKL 20101916021

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SANYMED S.A.S

Country of Origin

Italy

Authorized Representative

PT. PERFECT MEDILAB INDONESIA

AR Address

jl.Bunga Wijaya Kesuma Psr.IV No.11 Titi Rante

Registration Date

Mar 08, 2024

Expiry Date

Jan 10, 2029

Product Type

Clinical Chemistry Test System

Bilirubin (total or direct) test system (kit & cair)

Invitro Diagnostics

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