Taiwan FDA registration fd484cfca221abe49b98cb902b57152f

"Mico Air" manual surgical drill grip (unsterilized)

TW: “邁可艾爾”手動式外科鑽手握器 (未滅菌)

Taiwan·Risk Class 1·MicroAire Surgical Instruments, LLC·Registered May 06, 2013 – May 06, 2018Cancelled

Registration details

Analysis ID: fd484cfca221abe49b98cb902b57152f
Customs Code: DHA04401297409

Company information

Manufacturer: MicroAire Surgical Instruments, LLC
Manufacturer Country: United States
Authorized Representative: ENTMED CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the medical device management measures "Cranial drill mobile phone (K4325)".
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4325 Cranial drill handpiece
Import Information: import

Dates and status

Registration Date: May 06, 2013
Expiry Date: May 06, 2018
Cancellation Date: Aug 19, 2015

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Mico Air" manual surgical drill grip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd484cfca221abe49b98cb902b57152f and manufactured by MicroAire Surgical Instruments, LLC. The authorized representative in Taiwan is ENTMED CO., 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.