Taiwan FDA registration 1caf3d1d686797f9d6b308ba8afa836b
"Aon" drainage bottle (sterilized)
TW: "怡安" 引流瓶 (滅菌)
Registration details
- Analysis ID
- 1caf3d1d686797f9d6b308ba8afa836b
Company information
- Manufacturer
- LILY MEDICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Jun 28, 2010
- Expiry Date
- Jun 28, 2025
About this record
Access comprehensive regulatory information for "Aon" drainage bottle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1caf3d1d686797f9d6b308ba8afa836b and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is LILY MEDICAL 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.
Free DatabasePowered by Pure Global AI89,000+ Devices