"Bit Seal" blood collection pen (unsterilized)
Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jan 15, 2013 – Jan 15, 2018Cancelled- Analysis ID
- 97cec519d6e840e51028357f96880ee8
- Customs Code
- DHA04600182204
- Manufacturer Country
- China
- Authorized Representative
- Bit Seal Biotechnology Co., Ltd
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Chinese goods;; input
- Registration Date
- Jan 15, 2013
- Expiry Date
- Jan 15, 2018
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Bit Seal" 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 97cec519d6e840e51028357f96880ee8 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Bit Seal Biotechnology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GMMC, 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.