Identity
- Trade Name
- Adult Sotair Device FDA UDI
- Generic Name
- Airway pressure monitor, non-powered FDA UDI
- Device Name
- The Sotair™ device is a universal safety accessory device that is compatible with all manual resuscitators and airway interfaces that have standard ISO 5356-1:2015 15/22 mm connections. The device connects in-line between the bag and the mask, endotracheal tube or other applicable adjunct. In use, when the provider squeezes the bag too forcefully, crossing the maximum flow-limiting safety threshold of air delivered (~ 55 liters-per-minute), the Sotair device’s valve will instantaneously close. The valve remains closed as long as the user is maintaining the force of an unsafe squeeze on the bag. Once the provider releases the grip on the resuscitator bag, the valve will rapidly return to its resting position allowing the user to resume resuscitation at a safe flow. FDA UDI
- Model / Reference
- 00 FDA UDI
- Description
- The Sotair™ device is a universal safety accessory device that is compatible with all manual resuscitators and airway interfaces that have standard ISO 5356-1:2015 15/22 mm connections. The device connects in-line between the bag and the mask, endotracheal tube or other applicable adjunct. In use, when the provider squeezes the bag too forcefully, crossing the maximum flow-limiting safety threshold of air delivered (~ 55 liters-per-minute), the Sotair device’s valve will instantaneously close. The valve remains closed as long as the user is maintaining the force of an unsafe squeeze on the bag. Once the provider releases the grip on the resuscitator bag, the valve will rapidly return to its resting position allowing the user to resume resuscitation at a safe flow. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860006979607 FDA UDI
- 510(k) Number
- K212905 FDA UDI
- FDA Product Code
- BTM FDA UDI
- GMDN Term
- Airway pressure monitor, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5915 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Category: Airway pressure monitor, non-powered
Adult Sotair Device by Safe Bvm Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Safe Bvm Corporation
Sources (1)
- FDA UDI f69928db-a996-4bd3-a51d-8fb23e99b8a5 34 fields · synced May 30, 2026