Identity
- Trade Name
- XVAC FDA UDI
- Generic Name
- General-purpose suction system, pneumatic FDA UDI
- Model / Reference
- 100-120V FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04033817753070 FDA UDI
- 510(k) Number
- K110782 FDA UDI
- FDA Product Code
- CAC FDA UDI
- GMDN Term
- General-purpose suction system, pneumatic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5830 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose suction system, pneumatic
Xvac by LivaNova Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Furine — Furine ApS · Class I
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- VarioAir B BS — Drägerwerk AG & Co. KGaA · Class IIa
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
- LivaNova Deutschland GmbH
Sources (1)
- FDA UDI d6165517-365d-4b06-a00f-166b189518bb 33 fields · synced May 30, 2026