Taiwan FDA registration f70da78013b1fdceb399ab36d73a380f
"Ceracarta" Patient Lubricant (Non-sterile)
TW: "喜樂達" 病患用潤滑劑 (未滅菌)
Taiwan·Risk Class 1·MD·CERACARTA S.P.A·Registered Oct 05, 2015 – Oct 05, 2025ExpiredRegistration details
- Analysis ID
- f70da78013b1fdceb399ab36d73a380f
- License Form
- Ministry of Health Medical Device Import No. 015715
- Customs Code
- DHA09401571506
Company information
- Manufacturer
- CERACARTA S.P.A
- Manufacturer Country
- Italy
- Authorized Representative
- PAI LEA ENT. CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Lubricants for Patients (J.6375)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6375 Lubricant for patients
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 05, 2015
- Expiry Date
- Oct 05, 2025
About this record
Access comprehensive regulatory information for "Ceracarta" Patient Lubricant (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f70da78013b1fdceb399ab36d73a380f and manufactured by CERACARTA S.P.A. The authorized representative in Taiwan is PAI LEA ENT. CO., LTD..
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