FDA UDI
In Commercial Distribution
🇺🇸 United States
A.M.G.PMP PEDIATRIC
DI: 08052705493351
·
Model: A.M.G.PMP PEDIATRIC STERILE
·
EUROSETS SRL
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1
Basic Information
- Brand Name
- A.M.G.PMP PEDIATRIC
- Primary DI
- 08052705493351
- Version / Model
- A.M.G.PMP PEDIATRIC STERILE
- Catalog Number
- US5087
- Company Name
- EUROSETS SRL
- Labeler DUNS
- 439962374
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-02-19
- Public Version
- 1
- Public Version Date
- 2025-02-27
- Public Version Status
- New
- Public Device Record Key
- 43f21e1d-8954-456d-9e30-e6229a08d089
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- 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 |
|---|---|---|---|---|---|---|
| Package | 18052705493358 | GS1 | 1 | In Commercial Distribution | ||
| Primary | 08052705493351 | GS1 | ||||
| Package | 28052705493355 | GS1 | 4 | In Commercial Distribution |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K202206 | 000 |