Taiwan FDA registration 1be11baf2b7435a48669e5810e59b1a1

Pakjet Lancet (Unsterilized)

TW: 百捷 採血筆 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Ruikang Biomedical Co., Ltd. Precision Factory·Registered Oct 06, 2016 – Oct 06, 2026Active
Registration details
Analysis ID
1be11baf2b7435a48669e5810e59b1a1
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Oct 06, 2016
Expiry Date
Oct 06, 2026
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About this record

Access comprehensive regulatory information for Pakjet Lancet (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1be11baf2b7435a48669e5810e59b1a1 and manufactured by Ruikang Biomedical Co., Ltd. Precision Factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD., 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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