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"Meku" manual orthopedic surgical instruments (sterilized/unsterilized) - Taiwan Registration 65f75cdccd514f0b570d245ccc987462

Access comprehensive regulatory information for "Meku" manual orthopedic surgical instruments (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65f75cdccd514f0b570d245ccc987462 and manufactured by MAKO Surgical Corp.. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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65f75cdccd514f0b570d245ccc987462
Registration Details
Taiwan FDA Registration: 65f75cdccd514f0b570d245ccc987462
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Device Details

"Meku" manual orthopedic surgical instruments (sterilized/unsterilized)
TW: "็พŽ้…ท"ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

65f75cdccd514f0b570d245ccc987462

DHA09401409306

Company Information

United States

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

Apr 25, 2014

Apr 25, 2029