UDI device identifier
BD MAX Check-Points CPO 278102
UDI device identifier 00180002781029 · Check-Points Health B.V.
Key facts
| Primary DI | 00180002781029 |
|---|---|
| Brand name | BD MAX Check-Points CPO |
| Version or model | 278102 |
| Catalog number | 278102 |
| Company | Check-Points Health B.V. |
| DUNS number | 409613986 |
| Product code | POC |
| GMDN term | Multiple antimicrobial resistance nucleic acid IVD, kit, nucleic acid technique (NAT) |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 1, 2019 |
| Version date | Oct 1, 2025 |
| Description | BD MAX Check-Points CPO contains: 24 each, Master Mix, Reagent Strips, Extraction Tubes, Sample Buffer Tubes, Septum Caps. The BD MAX Check-Points CPO Assay detects the presence of carbapenemase genes in Gram-negative bacteria and includes an internal Sample Processing Control. |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: