Taiwan FDA registration 6307209061b5d8137fa8aaeda8d960bc

"Botong" blood collection needle (sterile)

TW: "博通"採血針(滅菌)
Taiwan flagTaiwan·Risk Class 1·Tianjin Huahong Technology Co., Ltd.·Registered Mar 03, 2015 – Mar 03, 2025Expired
Registration details
Analysis ID
6307209061b5d8137fa8aaeda8d960bc
Customs Code
DHA09600233708
Company information
Manufacturer Country
China
Authorized Representative
BROADMASTER BIOTECH. CORP.
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
Mar 03, 2015
Expiry Date
Mar 03, 2025
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About this record

Access comprehensive regulatory information for "Botong" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6307209061b5d8137fa8aaeda8d960bc and manufactured by Tianjin Huahong Technology Co., Ltd.. The authorized representative in Taiwan is BROADMASTER BIOTECH. CORP..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including STERILANCE MEDICAL (SUZHOU) INC., ANHUI KANGDA MEDICAL 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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