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XKIVD BCII-LYSE 500mL - Indonesia BPOM Medical Device Registration

XKIVD BCII-LYSE 500mL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208520033. The device is manufactured by ZHEJIANG XINKE MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SHARED TERRACE.

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
XKIVD BCII-LYSE 500mL
Analysis ID: AKL 20208520033

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SHARED TERRACE

AR Address

Jl. Radin Inten II No.7 Blok L-M

Registration Date

Feb 03, 2025

Expiry Date

Jun 12, 2028

Product Type

Hematological Reagents

Red cell lysing reagent.

Invitro Diagnostics

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