Identity
- Trade Name
- Integra EZ Oxygen Concentrator FDA UDI
- Generic Name
- Stationary oxygen concentrator FDA UDI
- Device Name
- Stationary Oxygen Concentrator 1-10 LPM, OM, 220 Volt FDA UDI
- Model / Reference
- 9621-SEQ FDA UDI
- Description
- Stationary Oxygen Concentrator 1-10 LPM, OM, 220 Volt FDA UDI
Identifiers
- Primary DI / UDI-DI
- M7669621SEQ0 FDA UDI
- 510(k) Number
- K042262 FDA UDI
- FDA Product Code
- CAW FDA UDI
- GMDN Term
- Stationary oxygen concentrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5440 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Stationary oxygen concentrator
Integra EZ Oxygen Concentrator by Caire Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Stationary oxygen concentrator.
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- NewLife Intensity — Airsep Corp. · Class II
- DeVilbiss — DeVilbiss Healthcare LLC. · Class II
- Oxygen Concentrator — Proactive Medical Products · Class II
- Inogen At Home Stationary Concentrator — Inogen, Inc. · Class II
Cleared under the same submission
K042262 also covers:
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
- Caire Inc.
Sources (1)
- FDA UDI c1e71cfe-1f00-4487-a6da-130a81590543 34 fields · synced May 30, 2026