Taiwan FDA registration e0ac5b194a8a0b40312eb70550065550
Bausch + Lomb ReNu Fresh Multi-Purpose Solution
TW: 博士倫瑞霖炫萌多效保養液
Taiwan·Risk Class 2·MD·Bausch & Lomb Incorporated·Registered May 28, 2015 – Oct 22, 2025ExpiredRegistration details
- Analysis ID
- e0ac5b194a8a0b40312eb70550065550
- License Form
- Ministry of Health Medical Device Import No. 027308
- Customs Code
- DHA05602730802
Company information
- Manufacturer
- Bausch & Lomb Incorporated
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5928 Flexible Contact Lens Preservation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2015
- Expiry Date
- Oct 22, 2025
About this record
Access comprehensive regulatory information for Bausch + Lomb ReNu Fresh Multi-Purpose Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0ac5b194a8a0b40312eb70550065550 and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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