VentStar Oxylog 3000F, 2000p 5x
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- VentStar Oxylog 3000F,2000p 5x EUDAMEDFDA UDI
- Generic Name
- Ventilator breathing circuit, single-use FDA UDI
- Model / Reference
- 5703041 EUDAMEDFDA UDI308030XK19Z000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04048675449119 EUDAMEDFDA UDI
- Basic UDI-DI
- 040486751308030XK19Z000DJ EUDAMED
- 510(k) Number
- K062267 FDA UDI
- FDA Product Code
- CBK FDA UDI
- EMDN Code
- R02010101 BREATHING CIRCUITS, W/O WATER TRAP EUDAMED
- GMDN Term
- Ventilator breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 868.5895 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Ventilator breathing circuit, single-use
VentStar Oxylog 3000F, 2000p 5x by Drägerwerk AG & Co. KGaA — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Cleared under the same submission
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Drägerwerk AG & Co. KGaA
Sources (2)
- FDA UDI 005cf179-d34d-45e4-bdce-0506c77b04b7 33 fields · synced Jul 24, 2026
- EUDAMED 9eb47e16-aff3-4638-a537-e973e8864512 61 fields · synced Jul 24, 2026