Pure Global

"Bereoti" magnifying glass and its accessories (unsterilized) - Taiwan Registration fefbf7252c3af0168c3930952ca3baac

Access comprehensive regulatory information for "Bereoti" magnifying glass and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fefbf7252c3af0168c3930952ca3baac and manufactured by PERIOPTIX INC.. The authorized representative in Taiwan is DENSO SCIENTIFIC 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 Database
Powered by Pure Global AI
89,000+ Devices
fefbf7252c3af0168c3930952ca3baac
Registration Details
Taiwan FDA Registration: fefbf7252c3af0168c3930952ca3baac
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bereoti" magnifying glass and its accessories (unsterilized)
TW: โ€œ่ฒ็‘žๆญๅ คโ€ๆ”พๅคง้กๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

fefbf7252c3af0168c3930952ca3baac

DHA04400659900

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Mar 24, 2008

Mar 24, 2013

Jun 03, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ