Identity
- Trade Name
- KIT DISPOSABLE RESPIRATORY CIRCUIT FDA UDI
- Generic Name
- Ventilator breathing circuit, single-use FDA UDI
- Device Name
- DUAL LIMB BREATHING CIRCUIT WITH UNIVERSAL FLOW SENSOR, FLOW SENSOR LINE, EXHALATION VALVE, DIAPHRAGM, AND HME FILTER FOR USE WITH OXYMAG, 1.5M, SINGLE-USE FDA UDI
- Model / Reference
- 1707816 FDA UDI
- Description
- DUAL LIMB BREATHING CIRCUIT WITH UNIVERSAL FLOW SENSOR, FLOW SENSOR LINE, EXHALATION VALVE, DIAPHRAGM, AND HME FILTER FOR USE WITH OXYMAG, 1.5M, SINGLE-USE FDA UDI
Identifiers
- Catalog Number
- 1707816 FDA UDI
- Primary DI / UDI-DI
- 07898671250168 FDA UDI
- FDA Product Code
- BZO FDA UDI
- GMDN Term
- Ventilator breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5975 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ventilator breathing circuit, single-use
Kit Disposable Respiratory Circuit by Magnamed Tecnologia Medica Sa — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Magnamed Tecnologia Medica Sa
Sources (1)
- FDA UDI 1c644231-d410-4d99-8de4-161b2758fe03 35 fields · synced May 30, 2026