UDI device identifier
Sureform 48230M
UDI device identifier 00886874121931 · INTUITIVE SURGICAL, INC.
Key facts
| Primary DI | 00886874121931 |
|---|---|
| Brand name | Sureform |
| Version or model | 48230M |
| Company | INTUITIVE SURGICAL, INC. |
| DUNS number | 938647021 |
| Product code | GDW |
| GMDN term | Surgical staple loading unit, non-cutting |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | May 11, 2022 |
| Version date | Aug 26, 2026 |
| Description | 8mm Stapler |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: