UDI device identifier
CODMAN® 261221
UDI device identifier 10381780513599 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Key facts
| Primary DI | 10381780513599 |
|---|---|
| Brand name | CODMAN® |
| Version or model | 261221 |
| Catalog number | 26-1221 |
| Company | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
| DUNS number | 081277700 |
| Product code | HBF |
| GMDN term | Automatic cranial perforator, single-use |
| Premarket submission | K791101 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 1, 2020 |
| Version date | Jun 24, 2025 |
| Description | CODMAN® Disposable Perforator 14mm |
At a glance
- 10–99 MAUDE reports citing this UDI
- Yes 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: