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"Central" orthopedic percutaneous minimally invasive scalpel (sterilized) - Taiwan Registration 61865f002967dfb14115155dcc0434f4

Access comprehensive regulatory information for "Central" orthopedic percutaneous minimally invasive scalpel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 61865f002967dfb14115155dcc0434f4 and manufactured by CENTRAL MEDICAL TECHNOLOGIES INC.. The authorized representative in Taiwan is CENTRAL MEDICAL TECHNOLOGIES INC..

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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61865f002967dfb14115155dcc0434f4
Registration Details
Taiwan FDA Registration: 61865f002967dfb14115155dcc0434f4
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Device Details

"Central" orthopedic percutaneous minimally invasive scalpel (sterilized)
TW: โ€œไธญๅคฎโ€้ชจ็ง‘็ถ“็šฎๅพฎๅ‰ตๆ‰‹่ก“ๅˆ€ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

61865f002967dfb14115155dcc0434f4

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.

N Orthopedics

N.4540 ๆ‰‹ๅ‹•ๅผ้ชจ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

May 08, 2012

May 08, 2017

Nov 18, 2019

Cancellation Information

Logged out

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