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SANSURE Sample Diluent - Indonesia BPOM Medical Device Registration

SANSURE Sample Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420302. The device is manufactured by SANSURE BIOTECH INC. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SANSURE BIOTECH 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 : A
SANSURE Sample Diluent
Analysis ID: AKL 10204420302

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SANSURE BIOTECH INDONESIA

AR Address

SANSURE BIOTECH INDONESIA

Registration Date

Dec 13, 2024

Expiry Date

Jul 30, 2029

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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