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SBM Keratoscope (Non-sterile) - Taiwan Registration eb1ccfbb24c59f0817d066308cf75a2d

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..

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.

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eb1ccfbb24c59f0817d066308cf75a2d
Registration Details
Taiwan FDA Registration: eb1ccfbb24c59f0817d066308cf75a2d
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Device Details

SBM Keratoscope (Non-sterile)
TW: ่ฆ–ๅฟ…ๆ˜Ž ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

eb1ccfbb24c59f0817d066308cf75a2d

Ministry of Health Medical Device Import Registration No. a00212

DHA084a0021202

Company Information

Italy

Product Details

Limited to the first level identification scope of the "corneoscopy (M.1350)" of the classification and grading management method for medical equipment.

M Ophthalmology

M1350 Keatoscope

Dates and Status

Aug 12, 2023

Oct 31, 2024