Taiwan FDA registration b2ebd3a99f3ace4bf68be7a1abc3dae5
Yaste capillary pipette (unsterilized)
TW: 亞斯特毛細微量吸管(未滅菌)
Taiwan·Risk Class 1·GLASWARENFABRIK KARL HECHT GMBH & CO. KG·Registered Oct 03, 2005 – Oct 03, 2025ExpiredRegistration details
- Analysis ID
- b2ebd3a99f3ace4bf68be7a1abc3dae5
- Customs Code
- DHA04400071600
Company information
- Manufacturer
- GLASWARENFABRIK KARL HECHT GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- NAN HO-SHING CO., LTD.
Product details
- Intended Use
- Blood is adsorbed into the capillary to facilitate comparative analysis of blood.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.6150 Capillary Blood Collection Tubes
- Import Information
- import
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 2025
About this record
Access comprehensive regulatory information for Yaste capillary pipette (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b2ebd3a99f3ace4bf68be7a1abc3dae5 and manufactured by GLASWARENFABRIK KARL HECHT GMBH & CO. KG. The authorized representative in Taiwan is NAN HO-SHING 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.
Free DatabasePowered by Pure Global AI89,000+ Devices