Taiwan FDA registration 3401a624b7df636e3fbe607708dd591d

"Medtronic" Bess spinal system

TW: “美敦力”倍斯脊椎系統
Taiwan flagTaiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Oct 30, 2007 – Oct 30, 2017Cancelled
Registration details
Analysis ID
3401a624b7df636e3fbe607708dd591d
Customs Code
DHA00601838207
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3070 椎弓螺釘系統
Import Information
import
Dates and status
Registration Date
Oct 30, 2007
Expiry Date
Oct 30, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Medtronic" Bess spinal system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3401a624b7df636e3fbe607708dd591d and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO, MEDTRONIC SOFAMOR DANEK MANUFACTURING, and 3 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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