UDI device identifier
Action® Bolx II
UDI device identifier 00089904000156 · ACTION PRODUCTS, INC.
Key facts
| Primary DI | 00089904000156 |
|---|---|
| Brand name | Action® |
| Version or model | Bolx II |
| Catalog number | 32102 |
| Company | ACTION PRODUCTS, INC. |
| DUNS number | 067543058 |
| Product code | JAD |
| GMDN term | Radiation therapy bolus, reusable |
| Premarket submission | K811528 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 21, 2016 |
| Version date | Mar 24, 2021 |
At a glance
- None 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: