Taiwan FDA registration cff1b27c4eae577954d7aa875603a448
“LabIVF” Rocket Craft Duo-Vac Suction Pump
TW: “磊柏”真空抽吸幫浦
Taiwan·Risk Class 2·MD·ROCKET MEDICAL·Registered Feb 05, 2015 – Feb 05, 2020CancelledRegistration details
- Analysis ID
- cff1b27c4eae577954d7aa875603a448
- License Form
- Ministry of Health Medical Device Import No. 027008
- Customs Code
- DHA05602700803
Company information
- Manufacturer
- ROCKET MEDICAL
- Manufacturer Country
- United Kingdom
- Authorized Representative
- LabIVF Taiwan International Co., Ltd
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6120 Assisted reproduction accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2015
- Expiry Date
- Feb 05, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “LabIVF” Rocket Craft Duo-Vac Suction Pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cff1b27c4eae577954d7aa875603a448 and manufactured by ROCKET MEDICAL. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.
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