SUCCEEDER D-Dimer Control Level II Lyophilized - Indonesia BPOM Medical Device Registration
SUCCEEDER D-Dimer Control Level II Lyophilized is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220225. The device is manufactured by BEIJING SUCCEEDER TECHNOLOGY INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is Rafa Topaz Main.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING SUCCEEDER TECHNOLOGY INC.Country of Origin
China
Authorized Representative
Rafa Topaz MainAR Address
Taman Buaran Indah I Blok U No. 242 Jl. Radin Inten II, Klender, Jakarta Timur
Registration Date
Sep 05, 2022
Expiry Date
Dec 31, 2025
Product Type
Hematological Reagents
Hematology quality control mixture.
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