Taiwan FDA registration be7db350f7773cdc11b0b1591470b839

Taibo sterilized blood lancet needle

TW: 泰博滅菌採血針
Taiwan flagTaiwan·Risk Class 1·BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.·Registered Oct 02, 2019 – Oct 02, 2029Active
Registration details
Analysis ID
be7db350f7773cdc11b0b1591470b839
Customs Code
DHA09600397302
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
Chinese goods;; Input;; QMS/QSD
Dates and status
Registration Date
Oct 02, 2019
Expiry Date
Oct 02, 2029
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About this record

Access comprehensive regulatory information for Taibo sterilized blood lancet needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be7db350f7773cdc11b0b1591470b839 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 TIANJIN HUAHONG TECHNOLOGY 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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