Taiwan FDA registration 2a6715be7c1bb9f23a4afa7748f2aace
“Lumendi” DiLumen Endolumenal Interventional Platform
TW: “羅曼迪”內視鏡手術通道
Taiwan·Risk Class 2·MD·LUMENDI, LLC·Registered Mar 31, 2022 – Mar 31, 2027ActiveRegistration details
- Analysis ID
- 2a6715be7c1bb9f23a4afa7748f2aace
- License Form
- Ministry of Health Medical Device Import No. 035370
- Customs Code
- DHA05603537003
Company information
- Manufacturer
- LUMENDI, LLC
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 31, 2022
- Expiry Date
- Mar 31, 2027
About this record
Access comprehensive regulatory information for “Lumendi” DiLumen Endolumenal Interventional Platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a6715be7c1bb9f23a4afa7748f2aace and manufactured by LUMENDI, LLC. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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