Taiwan FDA registration 897ec3fc6a493106d9ba3ef375362376
Turquoise coronary balloon dilation catheter
TW: 綠松石冠狀動脈氣球擴張導管
Taiwan·Risk Class 3·ALVIMEDICA TİBBİ Urunler SAN. AND EXTERNAL. T.C. Inc.·Registered Dec 12, 2011 – Dec 12, 2016CancelledRegistration details
- Analysis ID
- 897ec3fc6a493106d9ba3ef375362376
- Customs Code
- DHA00602310909
Company information
- Manufacturer Country
- Türkiye
- Authorized Representative
- JENS MEDICAL CONSULTING LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0005.
- Import Information
- import
Dates and status
- Registration Date
- Dec 12, 2011
- Expiry Date
- Dec 12, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Turquoise coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 897ec3fc6a493106d9ba3ef375362376 and manufactured by ALVIMEDICA TİBBİ Urunler SAN. AND EXTERNAL. T.C. Inc.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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