Taiwan FDA registration 8c71b8531cb3c267b3f06b835c16bde4
"Philips" Kingway electronic colposcopy digital imaging system
TW: “飛利浦”金科威電子陰道鏡數位成像系統
Taiwan·Risk Class 2·Philips Goldway (Shenzhen) Industrial Inc.·Registered Nov 10, 2015 – Nov 10, 2020CancelledRegistration details
- Analysis ID
- 8c71b8531cb3c267b3f06b835c16bde4
- Customs Code
- DHA09200071205
Company information
- Manufacturer
- Philips Goldway (Shenzhen) Industrial Inc.
- Manufacturer Country
- China
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1630 Yin Mirror
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 10, 2015
- Expiry Date
- Nov 10, 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 "Philips" Kingway electronic colposcopy digital imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c71b8531cb3c267b3f06b835c16bde4 and manufactured by Philips Goldway (Shenzhen) Industrial Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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