Taiwan FDA registration 3ab0d89e264ec91fb8c9c218f1d955d2
"Jiahong" portable stretcher (unsterilized)
TW: “佳鴻”手提式擔架 (未滅菌)
Registration details
- Analysis ID
- 3ab0d89e264ec91fb8c9c218f1d955d2
- Customs Code
- DHA04600074000
Company information
- Manufacturer Country
- China
- 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 "Portable Stretcher (J.6900)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6900 Hand-held stretcher
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 08, 2009
- Expiry Date
- Jul 08, 2014
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jiahong" portable stretcher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3ab0d89e264ec91fb8c9c218f1d955d2 and manufactured by JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..
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