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"Jiemai" Surgical Device (Extinction/Incannificaculation) - Taiwan Registration e83f329fa223c0471143b1f5e022365d

Access comprehensive regulatory information for "Jiemai" Surgical Device (Extinction/Incannificaculation) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e83f329fa223c0471143b1f5e022365d and manufactured by ZIMMER CAS. The authorized representative in Taiwan is ZIMMER BIOMET 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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e83f329fa223c0471143b1f5e022365d
Registration Details
Taiwan FDA Registration: e83f329fa223c0471143b1f5e022365d
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Device Details

"Jiemai" Surgical Device (Extinction/Incannificaculation)
TW: "ๆท้‚" ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e83f329fa223c0471143b1f5e022365d

DHA09402325303

Company Information

Canada

Product Details

Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

Sep 21, 2023

Sep 21, 2028