Pure Global

"Siemens" San Dino Blue Cytoplasmin Reagent - Taiwan Registration 16dbd21bd6c23c711a25184c7d0e5557

Access comprehensive regulatory information for "Siemens" San Dino Blue Cytoplasmin Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16dbd21bd6c23c711a25184c7d0e5557 and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
16dbd21bd6c23c711a25184c7d0e5557
Registration Details
Taiwan FDA Registration: 16dbd21bd6c23c711a25184c7d0e5557
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" San Dino Blue Cytoplasmin Reagent
TW: โ€œ่ฅฟ้–€ๅญโ€ ่–ๅธ่ซพ ่—่ƒžๆผฟ็ด ่ฉฆๅŠ‘
Risk Class 2

Registration Details

16dbd21bd6c23c711a25184c7d0e5557

DHA05603489304

Company Information

Italy

Product Details

This product is used in vitro diagnostics with Atellica CH Analyzer to quantify the determination of cytplasma in serum and plasma by immunoturbidimetry.

C Immunology and microbiology

C.5210 ่—่ƒžๆผฟ็ด ๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Aug 17, 2021

Aug 17, 2026