Taiwan FDA registration 7f8f6e20b406dd593fcd22bcf4968310
“Philips” IntelliSpare Perinatal
TW: “飛利浦”產房資訊管理系統
Taiwan·Risk Class 2·MD·PHILIPS MEDICAL SYSTEMS·Registered Nov 14, 2013 – Nov 14, 2018CancelledRegistration details
- Analysis ID
- 7f8f6e20b406dd593fcd22bcf4968310
- License Form
- Ministry of Health Medical Device Import No. 025462
- Customs Code
- DHA05602546202
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L2740 Pre- and post-production monitoring system and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2013
- Expiry Date
- Nov 14, 2018
- 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” IntelliSpare Perinatal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f8f6e20b406dd593fcd22bcf4968310 and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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