Taiwan FDA registration d18d303cbdeaeef3f939ac84cd219b6d

"Medtronic" Crison vertebral body filler

TW: “美敦力”克里森椎體填充器
Taiwan flagTaiwan·Risk Class 2·MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·Registered Aug 06, 2009 – Aug 06, 2024Cancelled
Registration details
Analysis ID
d18d303cbdeaeef3f939ac84cd219b6d
Customs Code
DHA00602010206
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.3080 椎體間融合裝置
Import Information
import
Dates and status
Registration Date
Aug 06, 2009
Expiry Date
Aug 06, 2024
Cancellation Date
Sep 21, 2022
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Medtronic" Crison vertebral body filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d18d303cbdeaeef3f939ac84cd219b6d and manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH, 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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