Taiwan FDA registration b30b6c10f4c5bfb20f40fab319336464

"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 Jan 17, 2017 – Jan 17, 2022Expired
Registration details
Analysis ID
b30b6c10f4c5bfb20f40fab319336464
License Form
Ministry of Health Medical Device Import No. 017423
Customs Code
DHA09401742303
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
Jan 17, 2017
Expiry Date
Jan 17, 2022
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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 b30b6c10f4c5bfb20f40fab319336464 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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