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"Kehui" Manual Orthopaedic Surgical Device (Inverted Bacteria) - Taiwan Registration abb94b38dd60b04ddbfd4ddd594e9256

Access comprehensive regulatory information for "Kehui" Manual Orthopaedic Surgical Device (Inverted Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number abb94b38dd60b04ddbfd4ddd594e9256 and manufactured by CANWELL MEDICAL CO, LTD.. The authorized representative in Taiwan is HELE TECHNOLOGY 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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abb94b38dd60b04ddbfd4ddd594e9256
Registration Details
Taiwan FDA Registration: abb94b38dd60b04ddbfd4ddd594e9256
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Device Details

"Kehui" Manual Orthopaedic Surgical Device (Inverted Bacteria)
TW: "็ง‘ๆƒ " ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

abb94b38dd60b04ddbfd4ddd594e9256

DHA09600486300

Company Information

China

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

QMS/QSD;; Input;; Chinese goods

Dates and Status

Dec 26, 2023

Dec 26, 2028