Pure Global

"Merck" Enriched culture medium (Non-Sterile) - Taiwan Registration 50c1802f5703821f6e5ea0896db05168

Access comprehensive regulatory information for "Merck" Enriched culture medium (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50c1802f5703821f6e5ea0896db05168 and manufactured by MERCK KGAA. The authorized representative in Taiwan is MERCK LTD..

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
50c1802f5703821f6e5ea0896db05168
Registration Details
Taiwan FDA Registration: 50c1802f5703821f6e5ea0896db05168
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Merck" Enriched culture medium (Non-Sterile)
TW: "้ป˜ๅ…‹" ๅผทๅŒ–ๅŸน้คŠๅŸบ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

50c1802f5703821f6e5ea0896db05168

Ministry of Health Medical Device Import No. 021520

DHA09402152003

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Intensive Medium (C.2330)".

C Immunology and microbiology devices

C2330 fortified medium

Imported from abroad

Dates and Status

May 06, 2020

May 06, 2025