Taiwan FDA registration 89e8b616b7aa276e4b1973e1e83a9b6e

"Yanar" permanent sminin remover (unsterilized)

TW: “雅納爾”永久性士敏汀去除劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·L & R MANUFACTURING COMPANY·Registered Jun 15, 2006 – Jun 15, 2011Cancelled
Registration details
Analysis ID
89e8b616b7aa276e4b1973e1e83a9b6e
Customs Code
DHA04400471301
Company information
Manufacturer Country
United States
Authorized Representative
PANDA BROTHERS & CO., LTD.
Product details
Intended Use
It is limited to the scope of Level 1 identification of "Disinfectants for General Medical Devices (J.6890)" of the Administrative Measures for Medical Devices.
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.6890 Disinfectants for general medical equipment
Import Information
import
Dates and status
Registration Date
Jun 15, 2006
Expiry Date
Jun 15, 2011
Cancellation Date
Nov 04, 2011
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Yanar" permanent 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 89e8b616b7aa276e4b1973e1e83a9b6e 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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