Taiwan FDA registration eb1ccfbb24c59f0817d066308cf75a2d
SBM Keratoscope (Non-sterile)
TW: 視必明 角膜鏡 (未滅菌)
Taiwan·Risk Class 1·MD·SBM SISTEMI·Registered Aug 12, 2023 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- eb1ccfbb24c59f0817d066308cf75a2d
- License Form
- Ministry of Health Medical Device Import Registration No. a00212
- Customs Code
- DHA084a0021202
Company information
- Manufacturer
- SBM SISTEMI
- Manufacturer Country
- Italy
- Authorized Representative
- DreamHawk Vision Biotech, Inc.
Product details
- Intended Use
- Limited to the first level identification scope of the "corneoscopy (M.1350)" of the classification and grading management method for medical equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M1350 Keatoscope
Dates and status
- Registration Date
- Aug 12, 2023
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for SBM Keratoscope (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 eb1ccfbb24c59f0817d066308cf75a2d and manufactured by SBM SISTEMI. The authorized representative in Taiwan is DreamHawk Vision Biotech, Inc..
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