Taiwan FDA registration ba9f847af485317a1c18e555984149c1
"Jiahong" bath push bed (unsterilized)
TW: “佳鴻”洗澡推床 (未滅菌)
Taiwan·Risk Class 1·EAKOH ENTERPRISE·Registered Nov 29, 2007 – Nov 29, 2017CancelledRegistration details
- Analysis ID
- ba9f847af485317a1c18e555984149c1
- Customs Code
- DHA04400633301
Company information
- Manufacturer
- EAKOH ENTERPRISE
- Manufacturer Country
- Singapore
- Authorized Representative
- CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- import
Dates and status
- Registration Date
- Nov 29, 2007
- Expiry Date
- Nov 29, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jiahong" bath push 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 ba9f847af485317a1c18e555984149c1 and manufactured by EAKOH ENTERPRISE. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..
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