Taiwan FDA registration 6f7e2dcccf9e5655cdaa31bba5af0ab0
Cardiopulmonary function test recorder
TW: 心肺功能測試記錄器
Taiwan·QUINTON INSTRUMENT CO.·Registered Dec 29, 1989 – Dec 29, 1994CancelledRegistration details
- Analysis ID
- 6f7e2dcccf9e5655cdaa31bba5af0ab0
- Customs Code
- DHA00600578001
Company information
- Manufacturer
- QUINTON INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- Pomei Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- 0211 Pulmonary function tester
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 1989
- Expiry Date
- Dec 29, 1994
- Cancellation Date
- Oct 06, 1999
Cancellation information
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
About this record
Access comprehensive regulatory information for Cardiopulmonary function test recorder in Taiwan's medical device market through Pure Global AI's free database. is registered under number 6f7e2dcccf9e5655cdaa31bba5af0ab0 and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Pomei Enterprise Co., Ltd.
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