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"ALIFAX" Selective Supplements (Non-Sterile) - Taiwan Registration 067b04998b8561bbf5ff732730451fdc

Access comprehensive regulatory information for "ALIFAX" Selective Supplements (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 067b04998b8561bbf5ff732730451fdc and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., 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.

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067b04998b8561bbf5ff732730451fdc
Registration Details
Taiwan FDA Registration: 067b04998b8561bbf5ff732730451fdc
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Device Details

"ALIFAX" Selective Supplements (Non-Sterile)
TW: "่‰พๅˆฉ็ฆๆ–ฏ" ้ธๆ“‡ๆ€งๅŸน้คŠๅŸบๆทปๅŠ ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

067b04998b8561bbf5ff732730451fdc

Ministry of Health Medical Device Import No. 020336

DHA09402033605

Company Information

Italy

Product Details

Limited to the first level identification range of additives (C.2450) of the culture medium of the medical device management method.

C Immunology and microbiology devices

Additives to C2450 medium

Imported from abroad

Dates and Status

Apr 18, 2019

Apr 18, 2024