Taiwan FDA registration fac6bc3e5a552580be6e0b5bfac939d5

"REDA" Manual surgical instrument for general use (NON-STERILE)

TW: "銳答" 一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·REDA INSTRUMENTE (ASIA PACIFIC) PTE LTD·Registered Oct 28, 2016 – Oct 28, 2021Expired
Registration details
Analysis ID
fac6bc3e5a552580be6e0b5bfac939d5
License Form
Ministry of Health Medical Device Import No. 017135
Customs Code
DHA09401713501
Company information
Manufacturer Country
Singapore
Authorized Representative
PRO-READY ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 28, 2016
Expiry Date
Oct 28, 2021
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About this record

Access comprehensive regulatory information for "REDA" Manual surgical instrument for general use (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fac6bc3e5a552580be6e0b5bfac939d5 and manufactured by REDA INSTRUMENTE (ASIA PACIFIC) PTE LTD. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including REDA INSTRUMENTE GMBH, 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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