Taiwan FDA registration 0fae04b1c5e384e2aef76a1240218684
“Unimax” Endometrial Cell Sampler
TW: “普威”子宮內膜刮器
Taiwan·Risk Class 2·MD·Puwei International Co., Ltd. Yilan Factory·Registered Feb 24, 2014 – Feb 24, 2024ExpiredRegistration details
- Analysis ID
- 0fae04b1c5e384e2aef76a1240218684
- License Form
- Ministry of Health Medical Device Manufacturing No. 004532
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1060 Endometrial aspirator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2024
About this record
Access comprehensive regulatory information for “Unimax” Endometrial Cell Sampler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fae04b1c5e384e2aef76a1240218684 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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