UDI device identifier
Infinion™ CX SC-2317-50
UDI device identifier M365SC2317500 · BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Key facts
| Primary DI | M365SC2317500 |
|---|---|
| Brand name | Infinion™ CX |
| Version or model | SC-2317-50 |
| Catalog number | SC-2317-50 |
| Company | BOSTON SCIENTIFIC NEUROMODULATION CORPORATION |
| DUNS number | 824951958 |
| Product code | LGW |
| GMDN term | Analgesic spinal cord electrical stimulation system |
| Premarket submission | P030017 |
| Device class | Class III |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2014 |
| Version date | Jul 6, 2018 |
| Description | Infinion CX, 50cm 16 Contact Lead Kit |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: