Taiwan FDA registration e529dfeb37d20e9824f4aae626627455
Yakruz Manual Patient Conveying Equipment ( Unsterilized)
TW: 雅克魯斯 手動病患輸送裝置 (未滅菌)
Taiwan·Risk Class 1·AKRUS GMBH &CO. KG·Registered Sep 15, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- e529dfeb37d20e9824f4aae626627455
- Customs Code
- DHA084a0011300
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 identification scope of the "Manual Patient Transport Device (J.6785)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6785 Manual Patient Conveying Device
Dates and status
- Registration Date
- Sep 15, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Yakruz Manual Patient Conveying Equipment ( Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e529dfeb37d20e9824f4aae626627455 and manufactured by AKRUS GMBH &CO. KG. The authorized representative in Taiwan is SUMTAGE ENTERPRISE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices