Taiwan FDA registration a07e8cc502e6ec87778bffd14dd3ab8b
"Philips" maternity room information management system
TW: “飛利浦” 產房資訊管理系統
Taiwan·Risk Class 2·Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC·Registered Mar 16, 2024 – Mar 16, 2029ActiveRegistration details
- Analysis ID
- a07e8cc502e6ec87778bffd14dd3ab8b
- Customs Code
- DHA05603694201
Company information
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.2740 Pre- and post-production monitoring systems and accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 16, 2024
- Expiry Date
- Mar 16, 2029
About this record
Access comprehensive regulatory information for "Philips" maternity room information management system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a07e8cc502e6ec87778bffd14dd3ab8b and manufactured by Philips Medizin Systeme Böblingen GmbH;; Philips North America LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices