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Fore blood pen (unsterilized) - Taiwan Registration c0a13cdb659018d982ed8a7558828f89

Access comprehensive regulatory information for Fore blood 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 c0a13cdb659018d982ed8a7558828f89 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, 2 companies making similar products including Taibo Technology Co., Ltd. five-stock factory, SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD., and 2 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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c0a13cdb659018d982ed8a7558828f89
Registration Details
Taiwan FDA Registration: c0a13cdb659018d982ed8a7558828f89
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Device Details

Fore blood pen (unsterilized)
TW: ็ฆ็ˆพๆŽก่ก€็ญ†(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c0a13cdb659018d982ed8a7558828f89

DHA09600389406

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

Jul 29, 2019

Jul 29, 2024