Identity
- Trade Name
- Nasal Alar SpO2 Sensor FDA UDI
- Generic Name
- Pulse oximeter probe, single-use FDA UDI
- Device Name
- Tri-anim, Nasal Alar SpO2 Sensor, 24/CS. Curaplex and Philips co-branded Nasal Alar single patient use multi-compatible SpO2 sensor. 24 sensors per case FDA UDI
- Model / Reference
- Tri-anim, Nasal SpO2 Sensor, 24/CS FDA UDI
- Description
- Tri-anim, Nasal Alar SpO2 Sensor, 24/CS. Curaplex and Philips co-branded Nasal Alar single patient use multi-compatible SpO2 sensor. 24 sensors per case FDA UDI
Identifiers
- Catalog Number
- 989803205401 FDA UDI
- Primary DI / UDI-DI
- 20884838097593 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pulse oximeter probe, single-use
Nasal Alar SpO2 Sensor by Philips Medical Systems Hsg — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Pulse oximeter probe, single-use.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Philips Medical Systems Hsg
Sources (1)
- FDA UDI 95ab891b-c4a6-4751-a2ec-7a29b671b89f 36 fields · synced Jun 8, 2026