FDA UDI
In Commercial Distribution
🇺🇸 United States
Oxevision Sleep system
DI: 50607514500023
·
Model: 2
·
OXEHEALTH LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Oxevision Sleep system
- Primary DI
- 50607514500023
- Version / Model
- 2
- Company Name
- OXEHEALTH LIMITED
- Labeler DUNS
- 218519521
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-01-21
- Public Version
- 1
- Public Version Date
- 2025-01-29
- Public Version Status
- New
- Public Device Record Key
- 87cd947d-0210-4bbf-9e46-5df03d80ed8d
Device Description
Sleep disorder interpretive software, professional-only
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| LEL | Device, Sleep Assessment | Neurology | 882.5050 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 64938 | Sleep disorder interpretive software, professional-only | An interpretive software program intended to be used exclusively by healthcare professionals to collect and analyse patient physiological data during sleep and publish reports to assist diagnosis of sleep disorders (e.g., insomnia, sleep apnoea). It is typically used as part of a polysomnography study using a wide range of data of [e.g., electrocardiogram (ECG), electroencephalogram (EEG), haemoglobin oxygen saturation (SpO2), chest wall motion, airflow, eye movement]. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 50607514500023 | GS1 |
Customer Contacts
- Phone
- +1 (888) 871-8108
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K233618 | 000 |