Taiwan FDA registration ae70b74912a643f8ef0a3154b6dad7b4

Fore Lancet (sterilized)

TW: 福爾 採血針 (滅菌)
Taiwan flagTaiwan·Risk Class 1·BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.·Registered Apr 02, 2018 – Apr 02, 2028Active
Registration details
Analysis ID
ae70b74912a643f8ef0a3154b6dad7b4
Customs Code
DHA09600338501
Company information
Manufacturer Country
China
Authorized Representative
TAIDOC TECHNOLOGY CORPORATION
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
Input;; Chinese goods;; QMS/QSD
Dates and status
Registration Date
Apr 02, 2018
Expiry Date
Apr 02, 2028
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About this record

Access comprehensive regulatory information for Fore Lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae70b74912a643f8ef0a3154b6dad7b4 and manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Qiaolian Technology Co., Ltd. Nankan No. 2 Factory, 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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