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"Aikman" modular shoulder humeral system - Taiwan Registration 516107ea0c0019bdcc572e0c075e21fe

Access comprehensive regulatory information for "Aikman" modular shoulder humeral system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 516107ea0c0019bdcc572e0c075e21fe and manufactured by ACUMED LLC.. The authorized representative in Taiwan is WONDERLAND CORPORATION.

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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516107ea0c0019bdcc572e0c075e21fe
Registration Details
Taiwan FDA Registration: 516107ea0c0019bdcc572e0c075e21fe
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Device Details

"Aikman" modular shoulder humeral system
TW: โ€œ่‰พๅ…‹ๆ›ผโ€ๆจก็ต„ๅŒ–่‚ฉ้—œ็ฏ€่‚ฑ้ชจ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

516107ea0c0019bdcc572e0c075e21fe

DHA00602088104

Company Information

United States

Product Details

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

N Orthopedics

N.3690 Shoulder joint humerus (half shoulder) metal type cement-type supplement

import

Dates and Status

Apr 06, 2010

Apr 06, 2015

Jun 08, 2018

Cancellation Information

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