Identity
- Trade Name
- Artema Anesthetic Oxygen (O2) Sensor FDA UDI
- Generic Name
- Respiratory oxygen sensor FDA UDI
- Model / Reference
- 989803162051 FDA UDI
Identifiers
- Catalog Number
- 989803162051 FDA UDI
- Primary DI / UDI-DI
- 00884838045286 FDA UDI
- FDA Product Code
- MWI FDA UDI
- GMDN Term
- Respiratory oxygen sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 FDA UDI
- Commercial Distribution
- 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Respiratory oxygen sensor
Artema Anesthetic Oxygen (O2) Sensor by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Respiratory oxygen sensor.
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- Vapotherm — Vapotherm Inc.
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 7653a4f8-45c3-46d6-aa27-1a7e29d2cdfc 34 fields · synced Jun 8, 2026