UDI device identifier
Bemis 3000
UDI device identifier 00073088149435 · BEMIS MANUFACTURING COMPANY
Key facts
| Primary DI | 00073088149435 |
|---|---|
| Brand name | Bemis |
| Version or model | 3000 |
| Catalog number | 3000 01; 3000 10 |
| Company | BEMIS MANUFACTURING COMPANY |
| DUNS number | 006072078 |
| Product code | KDQ |
| GMDN term | Surgical suction system collection container, reusable |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Nov 28, 2022 |
| Description | 3000CC REUSABLE OUTER CANISTER WITH PINK BRACKET FOR QUICK-FIT LINER SYSTEM |
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: