Singapore HSA registration DE0502549
Philips Nasal Alar SpO2 Sensor
Device classification
- Device Class
- CLASS C
- Medical Speciality Area
- General Hospital
Registration information
- Registration Number
- DE0502549
- Registration Date
- December 19, 2018
- Change Notification Approval Date
- November 12, 2024
- Retention Due Date
- December 18, 2025
Product description
The Nasal Alar SpO2™ Sensor is indicated for single patient use for continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate from the nasal ala of adult and pediatric patients, (at least 4 years and older and weighing > 15kg), who are well or poorly perfused. The sensor can be used in a variety of healthcare environments where compatible pulse oximetry monitors are indicated for use, under professional supervision.
Product Owner
- Short Name
- Philips
- Address
- 3000 Minuteman Road, Andover, MA 01810-1099, UNITED STATES
Registrant
- Address
- 622 LORONG 1 TOA PAYOH, SINGAPORE 319763
Importer
- Address
- 622 LORONG 1 TOA PAYOH, #L3-NA, SINGAPORE 319763
Model information
- Model Name(s)
- Nasal Alar SpO2 Sensor Nasal Alar SpO2 Sensor
- Model Identifier(s)
- 989803205381 989803205391
About this record
Access comprehensive regulatory information for Philips Nasal Alar SpO2 Sensor in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0502549 and owned by Philips Medical Systems. The device was registered on December 19, 2018.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS C