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"Taibo Burst" blood collection pen (unsterilized) - Taiwan Registration db19d189a143beefd803ca8a86c72495

Access comprehensive regulatory information for "Taibo Burst" 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 db19d189a143beefd803ca8a86c72495 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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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db19d189a143beefd803ca8a86c72495
Registration Details
Taiwan FDA Registration: db19d189a143beefd803ca8a86c72495
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Device Details

"Taibo Burst" blood collection pen (unsterilized)
TW: "ๆณฐๅš้€ฃ็™ผ"ๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

db19d189a143beefd803ca8a86c72495

DHA09600371200

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

Chinese goods;; input

Dates and Status

Mar 08, 2019

Mar 08, 2029