Taiwan FDA registration fe008ed469a9f35d8ae2285c5aa49a84
"Micro-Tech" Endoscope accessories (Sterile)
TW: "微創" 內視鏡附件 (滅菌)
Registration details
- Analysis ID
- fe008ed469a9f35d8ae2285c5aa49a84
- License Form
- Ministry of Health Medical Device Land Transport No. 002713
- Customs Code
- DHA09600271300
Company information
- Manufacturer
- MICRO-TECH(NANJING)CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- ERA BIOTEQ ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Endoscopes and Their Accessories (H.1500)".
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad; GMP;; Made in China
Dates and status
- Registration Date
- May 13, 2016
- Expiry Date
- May 13, 2026
About this record
Access comprehensive regulatory information for "Micro-Tech" Endoscope accessories (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe008ed469a9f35d8ae2285c5aa49a84 and manufactured by MICRO-TECH(NANJING)CO., LTD.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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