Taiwan FDA registration 61865f002967dfb14115155dcc0434f4

"Central" orthopedic percutaneous minimally invasive scalpel (sterilized)

TW: “中央”骨科經皮微創手術刀 (滅菌)

Taiwan·Risk Class 1·CENTRAL MEDICAL TECHNOLOGIES INC.·Registered May 08, 2012 – May 08, 2017Cancelled

Registration details

Analysis ID: 61865f002967dfb14115155dcc0434f4

Company information

Manufacturer: CENTRAL MEDICAL TECHNOLOGIES INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CENTRAL MEDICAL TECHNOLOGIES INC.

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4540 手動式骨科手術器械
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: May 08, 2012
Expiry Date: May 08, 2017
Cancellation Date: Nov 18, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

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..

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