Taiwan FDA registration 556140105adc2a119673f1b1d864d117

"TECNOWAY" Truncal orthosis (Non-Sterile)

TW: "鐵克諾威" 軀幹裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TECNOWAY SRL·Registered Jun 03, 2020 – Jun 03, 2025Cancelled
Registration details
Analysis ID
556140105adc2a119673f1b1d864d117
License Form
Ministry of Health Medical Device Import No. 021608
Customs Code
DHA09402160804
Company information
Manufacturer
TECNOWAY SRL
Manufacturer Country
Italy
Authorized Representative
LEADER MEDICAL INSTRUMENT CORPORATION
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3490 Torso Gear
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 03, 2020
Expiry Date
Jun 03, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "TECNOWAY" Truncal orthosis (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 556140105adc2a119673f1b1d864d117 and manufactured by TECNOWAY SRL. The authorized representative in Taiwan is LEADER MEDICAL INSTRUMENT CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TECNOWAY SRL, 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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