Pure Global

"Dybo" Liofilchem LEGIONELLA LATEX KIT (Non-sterile) - Taiwan Registration 636be8a7c05af60740c083c6a2abec2a

Access comprehensive regulatory information for "Dybo" Liofilchem LEGIONELLA LATEX KIT (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 636be8a7c05af60740c083c6a2abec2a and manufactured by LIOFILCHEM S. R. L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY 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
636be8a7c05af60740c083c6a2abec2a
Registration Details
Taiwan FDA Registration: 636be8a7c05af60740c083c6a2abec2a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Dybo" Liofilchem LEGIONELLA LATEX KIT (Non-sterile)
TW: "ๅธๅš"็ซ‹้ฃ›ๆ—‹้€€ไผ่ปไบบๆกฟ่Œๅฑฌไนณ่† ๅ‡้›†่ฉฆๅŠ‘ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

636be8a7c05af60740c083c6a2abec2a

Ministry of Health Medical Device Import No. 019771

DHA09401977100

Company Information

Italy

Product Details

Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.

C Immunology and microbiology devices

C3300 Haemophilus serology

Imported from abroad

Dates and Status

Nov 02, 2018

Nov 02, 2023