Taiwan FDA registration 54baf77bae1398a6f154386761c5ec34

"DIRECTA" Saliva absorber (Non-Sterile)

TW: "德瑞大" 唾液吸收片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DIRECTA AB·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
54baf77bae1398a6f154386761c5ec34
License Form
Ministry of Health Medical Device Import Registration No. 016535
Customs Code
DHA08401653500
Company information
Manufacturer
DIRECTA AB
Manufacturer Country
Sweden
Authorized Representative
YOUNG SUN DEVELOP CO.
Product details
Intended Use
Limited to the first level identification range of the "Saliva Absorber (F.6050)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F6050 Saliva absorber
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "DIRECTA" Saliva absorber (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 54baf77bae1398a6f154386761c5ec34 and manufactured by DIRECTA AB. The authorized representative in Taiwan is YOUNG SUN DEVELOP CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIRECTA AB, 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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