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"Semei" Tieca's anterior cervical lamina system - Taiwan Registration e1b6c329ad28a7d05dab7622e1c57b4a

Access comprehensive regulatory information for "Semei" Tieca's anterior cervical lamina system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1b6c329ad28a7d05dab7622e1c57b4a and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie Taiwan Co., Ltd..

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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e1b6c329ad28a7d05dab7622e1c57b4a
Registration Details
Taiwan FDA Registration: e1b6c329ad28a7d05dab7622e1c57b4a
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Device Details

"Semei" Tieca's anterior cervical lamina system
TW: "่ฅฟ็พŽ" ๆๅฐผๅกๅ‰ๆ–น้ ธๆคŽๆฟ็ณป็ตฑ
Risk Class 2

Registration Details

e1b6c329ad28a7d05dab7622e1c57b4a

DHA00601190800

Company Information

United States

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 14, 2005

Sep 14, 2025