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"Yanar" temporary sminin remover (unsterilized) - Taiwan Registration 56bcd9e1f20a2572576ac8f25c7e4213

Access comprehensive regulatory information for "Yanar" temporary sminin remover (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56bcd9e1f20a2572576ac8f25c7e4213 and manufactured by L & R MANUFACTURING COMPANY. The authorized representative in Taiwan is PANDA BROTHERS & CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including L & R MANUFACTURING COMPANY, and 1 recent registrations in the same category. 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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56bcd9e1f20a2572576ac8f25c7e4213
Registration Details
Taiwan FDA Registration: 56bcd9e1f20a2572576ac8f25c7e4213
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Device Details

"Yanar" temporary sminin remover (unsterilized)
TW: โ€œ้›…็ด็ˆพโ€ๆšซๆ™‚ๆ€งๅฃซๆ•ๆฑ€ๅŽป้™คๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

56bcd9e1f20a2572576ac8f25c7e4213

DHA04400471604

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".

J General hospital and personal use equipment

J.6890 Disinfectants for general medical equipment

import

Dates and Status

Jun 15, 2006

Jun 15, 2011

Nov 23, 2012

Cancellation Information

Logged out

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