Taiwan FDA registration 6f9ce97bfb3c50f9710c66e02077a839

"Elekoda" skull punch (unsterilized)

TW: “醫科達”顱骨打洞器 (未滅菌)

Taiwan·Risk Class 1·ELEKTA INSTRUMENT AB·Registered Feb 06, 2009 – Feb 06, 2024Expired

Registration details

Analysis ID: 6f9ce97bfb3c50f9710c66e02077a839
Customs Code: DHA04400745300

Company information

Manufacturer: ELEKTA INSTRUMENT AB
Manufacturer Country: Sweden
Authorized Representative: CHIU HO MEDICAL SYSTEM CO., LTD.

Product details

Intended Use: It is limited to the first level of identification of the "Cranial Cavern Punch (K.4750)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4750 Skull caving device
Import Information: import

Dates and status

Registration Date: Feb 06, 2009
Expiry Date: Feb 06, 2024

About this record

Access comprehensive regulatory information for "Elekoda" skull punch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6f9ce97bfb3c50f9710c66e02077a839 and manufactured by ELEKTA INSTRUMENT AB. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..

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