Taiwan FDA registration d97aeb7fee9dc554cf0b9d79b18a53f6
"Akrus" Manual Patient Transfer Device (Non-Sterile)
TW: "雅克魯斯" 手動病患輸送裝置 (未滅菌)
Taiwan·Risk Class 1·MD·AKRUS GMBH & CO. KG·Registered Jun 27, 2016 – Jun 27, 2021ExpiredRegistration details
- Analysis ID
- d97aeb7fee9dc554cf0b9d79b18a53f6
- License Form
- Ministry of Health Medical Device Import No. 016713
- Customs Code
- DHA09401671307
Company information
- Manufacturer
- AKRUS GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SUMTAGE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 27, 2016
- Expiry Date
- Jun 27, 2021
About this record
Access comprehensive regulatory information for "Akrus" Manual Patient Transfer Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d97aeb7fee9dc554cf0b9d79b18a53f6 and manufactured by AKRUS GMBH & CO. KG. The authorized representative in Taiwan is SUMTAGE ENTERPRISE CO., LTD..
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