Taiwan FDA registration 276c41bcb05fe1f62403c7bd2200cd53

Taibo sterilized blood lancet needle

TW: 泰博滅菌採血針
Taiwan flagTaiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Jun 05, 2019 – Jun 05, 2029Active
Registration details
Analysis ID
276c41bcb05fe1f62403c7bd2200cd53
Customs Code
DHA09600382500
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;; QMS/QSD;; Chinese goods
Dates and status
Registration Date
Jun 05, 2019
Expiry Date
Jun 05, 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 276c41bcb05fe1f62403c7bd2200cd53 and manufactured by TIANJIN HUAHONG TECHNOLOGY 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 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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