Taiwan FDA registration ba32d57ca8800c4081a6ffb8401c9378
Rebirth Pro2 Thrombus Aspiration Catheter
TW: 瑞伯斯普羅第二代血栓清除導管
Taiwan·Risk Class 2·MD·Goodman Co., LTD. Yamanashi Facility·Registered Dec 08, 2020 – Dec 08, 2025ExpiredRegistration details
- Analysis ID
- ba32d57ca8800c4081a6ffb8401c9378
- License Form
- Ministry of Health Medical Device Import No. 034211
- Customs Code
- DHA05603421104
Company information
- Manufacturer
- Goodman Co., LTD. Yamanashi Facility
- Manufacturer Country
- Japan
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 08, 2020
- Expiry Date
- Dec 08, 2025
About this record
Access comprehensive regulatory information for Rebirth Pro2 Thrombus Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba32d57ca8800c4081a6ffb8401c9378 and manufactured by Goodman Co., LTD. Yamanashi Facility. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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