Identity
- Trade Name
- VIRTUOX FDA UDI
- Generic Name
- Pulse oximeter, line-powered FDA UDI
- Device Name
- VIRTUOX Pulse Oximeter VPOD H PRO FDA UDI
- Model / Reference
- VPOD H PRO FDA UDI
- Description
- VIRTUOX Pulse Oximeter VPOD H PRO FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06942820462108 FDA UDI
- FDA Product Code
- DQA FDA UDI
- GMDN Term
- Pulse oximeter, line-powered 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pulse oximeter, line-powered
Virtuox by Beijing Choice Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pulse oximeter, line-powered.
- BCI — ICU MEDICAL, INC. · Class II
- Reusable Sensor - Y — MEDIAID INC · Class II
- Reusable Sensor - Ear — MEDIAID INC · Class II
- Unimed — Unimed Medical Supplies, Inc. · Class II
- BCI — ICU MEDICAL, INC. · Class II
- BCI — ICU MEDICAL, INC. · Class II
- Caring Mill — Caring Mill · Class II
- Reusable Sensor - Compushield (SCS) — MEDIAID INC · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Beijing Choice Electronic Technology Co., Ltd.
Sources (1)
- FDA UDI ad4e0908-bf64-4ea4-b0b5-8bf4533383f7 33 fields · synced May 30, 2026