UDI device identifier
Passio Redressing Kit PAS-02
UDI device identifier 00086000903220 · Bearpac Medical, LLC
Key facts
| Primary DI | 00086000903220 |
|---|---|
| Brand name | Passio Redressing Kit |
| Version or model | PAS-02 |
| Company | Bearpac Medical, LLC |
| DUNS number | 081178202 |
| Product code | DWM |
| GMDN term | Pleural/peritoneal drainage catheterization kit, non-medicated |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Feb 29, 2024 |
| Version date | Dec 15, 2025 |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: