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"Yanar" temporary sminin remover (unsterilized) - Taiwan Registration 6dc9df0bb48dd0fe19b92be1a2d6e79c

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 6dc9df0bb48dd0fe19b92be1a2d6e79c 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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6dc9df0bb48dd0fe19b92be1a2d6e79c
Registration Details
Taiwan FDA Registration: 6dc9df0bb48dd0fe19b92be1a2d6e79c
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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

6dc9df0bb48dd0fe19b92be1a2d6e79c

DHA04401098902

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

Oct 28, 2011

Oct 28, 2021

Sep 08, 2023

Cancellation Information

Logged out

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