Identity
- Trade Name
- CAREvent EMT FDA UDI
- Generic Name
- Pulmonary resuscitator, pneumatic, reusable FDA UDI
- Device Name
- The CAREvent EMT kit contains a CAREvent EMT resuscitator, a pressure regulator and an aspirator in moulded case with A Yankauer Suction Tip with Tubing. The CAREvent EMT hand held automatic resuscitator is pneumatically powered, time/volume cycled ventilatlatory resuscitator. It provides trained individuals with a safe and effective means of providing artificial ventilation during respiratory and cardiac arrest. The CAREvent EMT delivers automatic ventilation with controlled flow rates, airway pressure, tidal volume and frequencies. Patients are protected from over inflation and potential barotraumas by an audible Pressure Relief System. FDA UDI
- Model / Reference
- 01CV1112 FDA UDI
- Description
- The CAREvent EMT kit contains a CAREvent EMT resuscitator, a pressure regulator and an aspirator in moulded case with A Yankauer Suction Tip with Tubing. The CAREvent EMT hand held automatic resuscitator is pneumatically powered, time/volume cycled ventilatlatory resuscitator. It provides trained individuals with a safe and effective means of providing artificial ventilation during respiratory and cardiac arrest. The CAREvent EMT delivers automatic ventilation with controlled flow rates, airway pressure, tidal volume and frequencies. Patients are protected from over inflation and potential barotraumas by an audible Pressure Relief System. FDA UDI
Identifiers
- Catalog Number
- 01CV1112 FDA UDI
- Primary DI / UDI-DI
- 07540195025066 FDA UDI
- GMDN Term
- Pulmonary resuscitator, pneumatic, reusable FDA UDI
Classification
- 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pulmonary resuscitator, pneumatic, reusable
CAREvent EMT by O-Two Medical Technologies Inc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- SILICONE INFANT 280ML RESUSCITATOR W/ POP-OFF 40CM H2O — BESMED HEALTH BUSINESS CORP. · 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- O-Two Medical Technologies Inc
Sources (1)
- FDA UDI 4e36fbb2-b380-4aeb-8731-e8458dcdfa26 36 fields · synced May 30, 2026