UDI device identifier
GOMCO 02--01-0500
UDI device identifier 00026072002308 · Allied Medical, LLC
Key facts
| Primary DI | 00026072002308 |
|---|---|
| Brand name | GOMCO |
| Version or model | 02--01-0500 |
| Catalog number | 02-01-0500 |
| Company | Allied Medical, LLC |
| DUNS number | 119066872 |
| Product code | HFX |
| GMDN term | Surgical penis clamp, reusable |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 16, 2016 |
| Version date | Oct 13, 2025 |
| Description | 500 CIRC. CLAMP, NEW BORN 1.3 |
At a glance
- 1–9 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: