FDA UDI
In Commercial Distribution
🇺🇸 United States
Quantum Perfusion Blood Oxygenator with Integrated AF VT200-C2
DI: 08051160300709
·
Model: VT200-C2
·
SPECTRUM MEDICAL SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
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Basic Information
- Brand Name
- Quantum Perfusion Blood Oxygenator with Integrated AF VT200-C2
- Primary DI
- 08051160300709
- Version / Model
- VT200-C2
- Company Name
- SPECTRUM MEDICAL SRL
- Labeler DUNS
- 436188505
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2024-11-19
- Public Version
- 2
- Public Version Date
- 2025-09-11
- Public Version Status
- Update
- Public Device Record Key
- d09dd382-a4d9-41c5-89e8-3b6651f77bb3
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- Yes
- MRI Safety
- MR Unsafe
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DTZ | Oxygenator, Cardiopulmonary Bypass | Cardiovascular | 870.4350 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 17643 | Extracorporeal membrane oxygenator | A device designed for the extracorporeal diffusion of oxygen into blood across a gas-permeable membrane during a cardiopulmonary bypass or extracorporeal membrane oxygenation procedure. It includes a membrane that separates a thin layer of blood from the oxygenating gas; oxygen diffuses from the gas compartment into the blood, while carbon dioxide diffuses from the blood through the membrane and is flushed out of the oxygenator by the oxygen flow. The device may include an integrated heat exchanger, arterial filter, or cardiotomy/venous reservoir. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 08051160300709 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K212341 | 000 |