Taiwan FDA registration f0473a294bdde9cc18660c047c90e6d2
"Leo" three-stage expansion balloon tube
TW: “樂奧”三段擴張氣球導管
Taiwan·Risk Class 2·Leo Medical Co., Ltd.·Registered Mar 30, 2023 – Mar 30, 2028ActiveRegistration details
- Analysis ID
- f0473a294bdde9cc18660c047c90e6d2
- Customs Code
- DHA09200146506
Company information
- Manufacturer
- Leo Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5365 Esophageal extenders
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 30, 2023
- Expiry Date
- Mar 30, 2028
About this record
Access comprehensive regulatory information for "Leo" three-stage expansion balloon tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0473a294bdde9cc18660c047c90e6d2 and manufactured by Leo Medical Co., Ltd.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
This page provides complete technical specifications, regulatory compliance details. 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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