Pure Global

"Qiaolian" electrolyte analysis system - Taiwan Registration 02f15791ec5b8b3a5279feeaa41d6d4b

Access comprehensive regulatory information for "Qiaolian" electrolyte analysis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02f15791ec5b8b3a5279feeaa41d6d4b and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.

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
02f15791ec5b8b3a5279feeaa41d6d4b
Registration Details
Taiwan FDA Registration: 02f15791ec5b8b3a5279feeaa41d6d4b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Qiaolian" electrolyte analysis system
TW: "ๅ–ฌ่ฏ" ้›ป่งฃ่ณชๅˆ†ๆž็ณป็ตฑ
Risk Class 2

Registration Details

02f15791ec5b8b3a5279feeaa41d6d4b

Company Information

Taiwan, Province of China

Product Details

This product is intended for in vitro diagnostics by professionals for the quantitative determination of sodium, potassium, chloride and calcium in serum, plasma and whole blood.

A Clinical chemistry and clinical toxicology

A.1145 ้ˆฃ่ฉฆ้ฉ—็ณป็ตฑ;; A.1665 ้ˆ‰่ฉฆ้ฉ—็ณป็ตฑ;; A.0002 ่‡จๅบŠๅŒ–ๅญธ้›ขๅญๅˆ†ๆžๅ„€

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jun 13, 2024

Jun 13, 2029