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"Teifu Xin Disi Spine" Manual osteologic surgical instrument (sterile/unsterilized) - Taiwan Registration cea61f2797c0c915153d6eeb631f13c8

Access comprehensive regulatory information for "Teifu Xin Disi Spine" Manual osteologic surgical 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 cea61f2797c0c915153d6eeb631f13c8 and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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cea61f2797c0c915153d6eeb631f13c8
Registration Details
Taiwan FDA Registration: cea61f2797c0c915153d6eeb631f13c8
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Device Details

"Teifu Xin Disi Spine" Manual osteologic surgical instrument (sterile/unsterilized)
TW: "ๅธๅฏŒไฟก่ฟชๆ€่„ŠๆคŽ" ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cea61f2797c0c915153d6eeb631f13c8

DHA09402103002

Company Information

Switzerland

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

Nov 21, 2019

Nov 21, 2029