Pure Global

Ganoderma lucidum ecstasy enzyme immune reagent - Taiwan Registration 95b9e1826637085a9d403e41bcb6e2b8

Access comprehensive regulatory information for Ganoderma lucidum ecstasy enzyme immune reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 95b9e1826637085a9d403e41bcb6e2b8 and manufactured by LIN-ZHI INTERNATIONAL, INC. The authorized representative in Taiwan is TAIWAN ADVANCE BIO-PHARMACEUTICAL INC..

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
95b9e1826637085a9d403e41bcb6e2b8
Registration Details
Taiwan FDA Registration: 95b9e1826637085a9d403e41bcb6e2b8
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Ganoderma lucidum ecstasy enzyme immune reagent
TW: ้ˆ่Šๆ–้ ญไธธ้…ต็ด ๅ…็–ซ่ฉฆๅŠ‘
Risk Class 2

Registration Details

95b9e1826637085a9d403e41bcb6e2b8

DHA05603172701

Company Information

United States

Product Details

This product is used for the qualitative or semi-quantitative determination of ecstasy content in human urine.

A Clinical chemistry and clinical toxicology

A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products;; A.3610 ็”ฒๅŸบๅฎ‰้žไป–ๅ‘ฝ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Oct 11, 2018

Oct 11, 2028