UDI device identifier
Medline Industries, Inc. DYNJ0778497F
UDI device identifier 10195327563561 · MEDLINE INDUSTRIES, INC.
Key facts
| Primary DI | 10195327563561 |
|---|---|
| Brand name | Medline Industries, Inc. |
| Version or model | DYNJ0778497F |
| Catalog number | DYNJ0778497F |
| Company | MEDLINE INDUSTRIES, INC. |
| DUNS number | 025460908 |
| Product code | KDD |
| GMDN term | General surgical procedure kit, non-medicated, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 11, 2023 |
| Version date | Dec 19, 2023 |
| Description | HEART BASIN PACK-LF |
At a glance
- None MAUDE reports citing this UDI
- No 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: