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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 10204220350. 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. UBC MEDICAL 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 10204220350

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Aug 21, 2024

Expiry Date

May 23, 2026

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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