Pure Global

DYMIND Clotting Tetrachoric Combined Testing Kit (Coagulation Method) - Indonesia BPOM Medical Device Registration

DYMIND Clotting Tetrachoric Combined Testing Kit (Coagulation Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420016. The device is manufactured by SHENZEN DYMIND BIOTECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DYMIND 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
DYMIND Clotting Tetrachoric Combined Testing Kit (Coagulation Method)
Analysis ID: AKL 20207420016

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DYMIND BIOTECH INDONESIA

AR Address

DYMIND BIOTECH INDONESIA

Registration Date

Mar 05, 2024

Expiry Date

Feb 28, 2028

Product Type

Haematology Package and Kit

Partial thromboplastin time tests.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing