Taiwan FDA registration a3b5c1fafc1829b6b2d380371a74d296
“TRACOE” Aeris Balloon Dilation Catheter
TW: “創可”艾瑞絲氣囊擴張導管
Taiwan·Risk Class 2·MD·TRACOE medical GmbH·Registered Mar 15, 2019 – Mar 15, 2024ExpiredRegistration details
- Analysis ID
- a3b5c1fafc1829b6b2d380371a74d296
- License Form
- Ministry of Health Medical Device Import No. 032332
- Customs Code
- DHA05603233206
Company information
- Manufacturer
- TRACOE medical GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- Huixing Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4680 Bronchoscope (soft or rigid) and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 15, 2019
- Expiry Date
- Mar 15, 2024
About this record
Access comprehensive regulatory information for “TRACOE” Aeris Balloon Dilation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3b5c1fafc1829b6b2d380371a74d296 and manufactured by TRACOE medical GmbH. The authorized representative in Taiwan is Huixing Co., Ltd.
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