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O'Choice demineralized bony pnotation - Taiwan Registration b5e71b7eeed4cfa9f39718737eb02198

Access comprehensive regulatory information for O'Choice demineralized bony pnotation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5e71b7eeed4cfa9f39718737eb02198 and manufactured by Xtant Medical Holdings, Inc.. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL 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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b5e71b7eeed4cfa9f39718737eb02198
Registration Details
Taiwan FDA Registration: b5e71b7eeed4cfa9f39718737eb02198
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Device Details

O'Choice demineralized bony pnotation
TW: ๆญ็‰น้ธๅŽป็คฆๅŒ–่ฃœ้ชจ็‰ฉ
Risk Class 2

Registration Details

b5e71b7eeed4cfa9f39718737eb02198

DHA00602368802

Company Information

United States

Product Details

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

N Orthopedics

N.3045 Absorbable Calcium Salt Bone Cavity Filling Device

import

Dates and Status

Jun 26, 2012

Jun 26, 2027