Taiwan FDA registration 96ab85174143a0ae35adfcce703fd5da

"SPINEART" Orthopedic manual surgical instrument (Non-Sterile)

TW: "司百特" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SPINEART SA·Registered Feb 02, 2018 – Feb 02, 2023Expired
Registration details
Analysis ID
96ab85174143a0ae35adfcce703fd5da
License Form
Ministry of Health Medical Device Import No. 018789
Customs Code
DHA09401878901
Company information
Manufacturer
SPINEART SA
Manufacturer Country
Switzerland
Authorized Representative
JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
Intended Use
Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
N Orthopedic devices
Product Type (Level 2)
N4540 Manual osteologic surgery instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 02, 2018
Expiry Date
Feb 02, 2023
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About this record

Access comprehensive regulatory information for "SPINEART" Orthopedic manual surgical instrument (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 96ab85174143a0ae35adfcce703fd5da and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SPINEART SA, SPINEART, and 2 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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