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"Byott" tear test strip (unsterilized) - Taiwan Registration b8d29e1e2401e13f7f518de0a0fdddfb

Access comprehensive regulatory information for "Byott" tear test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b8d29e1e2401e13f7f518de0a0fdddfb and manufactured by BIOTECH VISION CARE PVT LTD. The authorized representative in Taiwan is Shanghua Industrial 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.

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b8d29e1e2401e13f7f518de0a0fdddfb
Registration Details
Taiwan FDA Registration: b8d29e1e2401e13f7f518de0a0fdddfb
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Device Details

"Byott" tear test strip (unsterilized)
TW: โ€œๆ‹œๆญ็‰นโ€ๆทšๆถฒ่ฉฆ็ด™ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b8d29e1e2401e13f7f518de0a0fdddfb

DHA04400645206

Company Information

Product Details

Limited to the first level recognition range of Schirmer test strip (M.1800) for the management of medical devices.

M Ophthalmology

M.1800 Schirmer่ฉฆ็ด™

import

Dates and Status

Jan 09, 2008

Jan 09, 2013

Apr 24, 2015

Cancellation Information

Logged out

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