Taiwan FDA registration 28c805c9b79e3c1217a0c29704cc8a97

"SCIFIT" Mechanical chair (Non-Sterile)

TW: "賽菲特"機械椅 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SCIFIT SYSTEMS INC·Registered Mar 23, 2016 – Mar 23, 2021Expired
Registration details
Analysis ID
28c805c9b79e3c1217a0c29704cc8a97
License Form
Ministry of Health Medical Device Import No. 016306
Customs Code
DHA09401630607
Company information
Manufacturer
SCIFIT SYSTEMS INC
Manufacturer Country
United States
Authorized Representative
GOOD LINE INCORPORATION
Product details
Intended Use
Limited to the first level identification scope of the "Mechanical Chair (O.3100)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3100 機械椅
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 23, 2016
Expiry Date
Mar 23, 2021
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About this record

Access comprehensive regulatory information for "SCIFIT" Mechanical chair (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 28c805c9b79e3c1217a0c29704cc8a97 and manufactured by SCIFIT SYSTEMS INC. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCIFIT SYSTEMS INC, 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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