Taiwan FDA registration 8960bfeda28b27987a7c984faca6b2c9

"Aitaka" Microbial Sample Collection and Delivery Equipment (Sterilization)

TW: "艾塔卡" 微生物樣本收集及輸送器材(滅菌)
Taiwan flagTaiwan·Risk Class 1·Aptaca S.p.A.·Registered Jan 31, 2024 – Jan 31, 2029Active
Registration details
Analysis ID
8960bfeda28b27987a7c984faca6b2c9
Customs Code
DHA09402338405
Company information
Manufacturer
Aptaca S.p.A.
Manufacturer Country
Italy
Authorized Representative
DiaTech Technology Co., Ltd.
Product details
Intended Use
Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.2900 Microbial sample collection and delivery equipment
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jan 31, 2024
Expiry Date
Jan 31, 2029
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About this record

Access comprehensive regulatory information for "Aitaka" Microbial Sample Collection and Delivery Equipment (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8960bfeda28b27987a7c984faca6b2c9 and manufactured by Aptaca S.p.A.. The authorized representative in Taiwan is DiaTech Technology Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Aptaca S.p.A, and 1 recent registrations in the same category. 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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