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SpO2 SENSOR GRIP ADULT/NEONATAL 2 PACK -989803162501
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- SpO2 SENSOR GRIP ADULT/NEONATAL 2 PACK -989803162501 FDA UDI
- Generic Name
- Pulse oximeter probe, reusable FDA UDI
- Device Name
- SpO2 Sensor Grip Adult/Neonatal 2 Pack FDA UDI
- Model / Reference
- SPO2 Sensor Grip, Adult/Neonatal 2 pack FDA UDI
- Description
- SpO2 Sensor Grip Adult/Neonatal 2 Pack FDA UDI
Identifiers
- Catalog Number
- 989803162501 FDA UDI
- Primary DI / UDI-DI
- 00884838034716 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter probe, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2700 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
A comprehensive 2-3 paragraph SEO description written in clear, natural language. This pulse oximeter probe is designed to be applied externally to a body site for the transcutaneous measurement of haemoglobin oxygen saturation (SpO2) in arterial blood.
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 DS North America LLC
Sources (1)
- FDA UDI 134a17d5-9b9b-49a8-9f4b-225cd8ebe72c 37 fields · synced Oct 6, 2026