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"Medtronic" Crison vertebral body filler - Taiwan Registration d18d303cbdeaeef3f939ac84cd219b6d

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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d18d303cbdeaeef3f939ac84cd219b6d
Registration Details
Taiwan FDA Registration: d18d303cbdeaeef3f939ac84cd219b6d
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Device Details

"Medtronic" Crison vertebral body filler
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅ…‹้‡ŒๆฃฎๆคŽ้ซ”ๅกซๅ……ๅ™จ
Risk Class 2
Cancelled

Registration Details

d18d303cbdeaeef3f939ac84cd219b6d

DHA00602010206

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order.

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

import

Dates and Status

Aug 06, 2009

Aug 06, 2024

Sep 21, 2022

Cancellation Information

Logged out

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