Taiwan FDA registration 308ada0764e5640d8ab1cc2afed8c82d
"Geelu" manually adjustable bed (unsterilized)
TW: "吉律" 手動可調整式病床(未滅菌)
Taiwan·Risk Class 1·KUNSHAN KAWAZA MEDICAL PRODUCTS CO., LTD.·Registered Nov 29, 2012 – Nov 29, 2017CancelledRegistration details
- Analysis ID
- 308ada0764e5640d8ab1cc2afed8c82d
- Customs Code
- DHA04600180201
Company information
- Manufacturer
- KUNSHAN KAWAZA MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GENEMAX MEDICAL PRODUCTS INDUSTRY CORP.
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Manual Adjustable Hospital Bed (J.5120)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5120 手動可調整式病床
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 29, 2012
- Expiry Date
- Nov 29, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Geelu" manually adjustable bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 308ada0764e5640d8ab1cc2afed8c82d and manufactured by KUNSHAN KAWAZA MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is GENEMAX MEDICAL PRODUCTS INDUSTRY CORP..
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