Taiwan FDA registration 2cd27aaaa001fb1f6765ad9a5191dcf8

Urolon

TW: 優而朗植入劑
Taiwan flagTaiwan·Risk Class 3·MD·AQLANE Medical B.V.·Registered Jun 26, 2023 – Jun 26, 2028Active
Registration details
Analysis ID
2cd27aaaa001fb1f6765ad9a5191dcf8
License Form
Ministry of Health Medical Device Import No. 036259
Customs Code
DHA05603625903
Company information
Manufacturer Country
Netherlands
Authorized Representative
CLOVERS BIOTECHNOLOGY CO., LTD.
Product details
Intended Use
This product is suitable for filling soft tissue treatment for the treatment of mild to moderate stress urinary incontinence (SUI) in adult women.
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H9999 Other
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 26, 2023
Expiry Date
Jun 26, 2028
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About this record

Access comprehensive regulatory information for Urolon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2cd27aaaa001fb1f6765ad9a5191dcf8 and manufactured by AQLANE Medical B.V.. The authorized representative in Taiwan is CLOVERS BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HAW LOONG ENTERPRISE 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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