Identity
- Trade Name
- RESPOND Ventilator Cart FDA UDI
- Generic Name
- Transport electric ventilator FDA UDI
- Model / Reference
- RESPOND Ventilator Cart FDA UDI
Identifiers
- Catalog Number
- 91-101-US207 FDA UDI
- Primary DI / UDI-DI
- 00850057117097 FDA UDI
- 510(k) Number
- K241135 FDA UDI
- FDA Product Code
- CBK FDA UDI
- GMDN Term
- Transport electric ventilator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5895 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Transport electric ventilator
RESPOND Ventilator Cart by Corvent Medical, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Transport electric ventilator.
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- VENT — Zoll Medical Corporation · Class II
- PATIENT CIRCUITS — Zoll Medical Corporation · Class II
- Z Vent — Zoll Medical Corporation · Class II
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- Bio-Med Devices, Inc. — Bio-Med Devices, Inc. · Class II
Cleared under the same submission
K241135 also covers:
- BV Filters — CORVENT MEDICAL, INC
- Cart, Accessory Bar — CORVENT MEDICAL, INC
- Cart, Display Bracket — CORVENT MEDICAL, INC
- Cart, Display Mount — CORVENT MEDICAL, INC
- Cart, Humidifier Mount — CORVENT MEDICAL, INC
- Cart, IV Pole — CORVENT MEDICAL, INC
- Cart, IV Pole Mount — CORVENT MEDICAL, INC
- Cart, Nebulizer Mount — CORVENT MEDICAL, INC
- Circuit Arm — CORVENT MEDICAL, INC
- Exhalation Valve — CORVENT MEDICAL, INC
- Flow Sensor Cable — CORVENT MEDICAL, INC
- Flow Sensors — CORVENT MEDICAL, INC
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
- Corvent Medical, Inc
Sources (1)
- FDA UDI 616096c7-d210-430b-b08b-c96cc5f123ab 35 fields · synced May 31, 2026