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"Kunibi" Manual Osteologic Surgery Instrument (Sterile/Unsterilized) - Taiwan Registration b558e13c5e9c0b546d8bdc5ae6944ccf

Access comprehensive regulatory information for "Kunibi" Manual Osteologic Surgery Instrument (Sterile/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b558e13c5e9c0b546d8bdc5ae6944ccf and manufactured by BIOMET UK LIMITED. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOMET ORTHOPEDICS, and 1 recent registrations in the same category. 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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b558e13c5e9c0b546d8bdc5ae6944ccf
Registration Details
Taiwan FDA Registration: b558e13c5e9c0b546d8bdc5ae6944ccf
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Device Details

"Kunibi" Manual Osteologic Surgery Instrument (Sterile/Unsterilized)
TW: "้‚ฆ็พŽ" ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b558e13c5e9c0b546d8bdc5ae6944ccf

DHA09401674800

Company Information

United Kingdom

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

Jul 06, 2016

Jul 06, 2026

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