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"Lianxian" blood collection pen (unsterilized) - Taiwan Registration 63d72c09e6e636c60d0c902857ccac9d

Access comprehensive regulatory information for "Lianxian" blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 63d72c09e6e636c60d0c902857ccac9d and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is LEISON BIOTECH 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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63d72c09e6e636c60d0c902857ccac9d
Registration Details
Taiwan FDA Registration: 63d72c09e6e636c60d0c902857ccac9d
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Device Details

"Lianxian" blood collection pen (unsterilized)
TW: "้€ฃ้™ž" ๆŽก่ก€็ญ† (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

63d72c09e6e636c60d0c902857ccac9d

DHA09600327201

Company Information

Product Details

Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Input;; Chinese goods

Dates and Status

Nov 16, 2017

Nov 16, 2027