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"Spite" lumbar intervertebral disc implants - Taiwan Registration 55149ee96c3b8358f6399fc98277083b

Access comprehensive regulatory information for "Spite" lumbar intervertebral disc implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55149ee96c3b8358f6399fc98277083b and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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55149ee96c3b8358f6399fc98277083b
Registration Details
Taiwan FDA Registration: 55149ee96c3b8358f6399fc98277083b
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Device Details

"Spite" lumbar intervertebral disc implants
TW: โ€œๅธไฝฐ็‰นโ€่…ฐๆคŽๆคŽ้–“็›คๆคๅ…ฅ็‰ฉ
Risk Class 2
Cancelled

Registration Details

55149ee96c3b8358f6399fc98277083b

DHA00602148300

Company Information

Switzerland

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

import

Dates and Status

Sep 23, 2010

Sep 23, 2020

Jun 07, 2022

Cancellation Information

Logged out

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