Taiwan FDA registration 939de81728402cd5e56b64decfde339e
"Irvine" Assisted Reproductive Technology Medium System
TW: "歐文"輔助生殖技術試劑系統
Taiwan·Risk Class 2·MD·FUJIFILM Irvine Scientific, Inc.·Registered Feb 15, 2022 – Feb 15, 2027ActiveRegistration details
- Analysis ID
- 939de81728402cd5e56b64decfde339e
- License Form
- Ministry of Health Medical Device Import No. 035307
- Customs Code
- DHA05603530709
Company information
- Manufacturer
- FUJIFILM Irvine Scientific, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- LabIVF Taiwan International Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L6180 Reproductive vehicles and supplements
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 15, 2022
- Expiry Date
- Feb 15, 2027
About this record
Access comprehensive regulatory information for "Irvine" Assisted Reproductive Technology Medium System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 939de81728402cd5e56b64decfde339e and manufactured by FUJIFILM Irvine Scientific, Inc.. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.
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