Taiwan FDA registration 58a36d64d42e522d311fbd6b11df08ac
“ROHTO” NEO EYE Aspheric Foldable Lens
TW: “樂敦”新視非球面人工水晶體
Taiwan·Risk Class 3·MD·PT Rohto Laboratories Indonesia·Registered Feb 24, 2014 – Feb 24, 2024ExpiredRegistration details
- Analysis ID
- 58a36d64d42e522d311fbd6b11df08ac
- License Form
- Ministry of Health Medical Device Import No. 025821
- Customs Code
- DHA05602582104
Company information
- Manufacturer
- PT Rohto Laboratories Indonesia
- Manufacturer Country
- Indonesia
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL CO., LTD.
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)
- M3600 intraocular lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2024
About this record
Access comprehensive regulatory information for “ROHTO” NEO EYE Aspheric Foldable Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 58a36d64d42e522d311fbd6b11df08ac and manufactured by PT Rohto Laboratories Indonesia. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL 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