UDI device identifier
Interventional Workspot Interventional Workspot - 1
UDI device identifier 00884838059191 · Philips Medical Systems Nederland B.V.
Key facts
| Primary DI | 00884838059191 |
|---|---|
| Brand name | Interventional Workspot |
| Version or model | Interventional Workspot - 1 |
| Catalog number | 001000 |
| Company | Philips Medical Systems Nederland B.V. |
| DUNS number | 413819707 |
| Product code | LLZ |
| GMDN term | Cardiovascular fluoroscopy/intravascular imaging software |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Sep 4, 2026 |
| Description | Software medical device hosting platform, used with a Philips Interventional X-Ray System. Provides common functionalities (e.g. import / export, data handling) for other software medical devices. |
At a glance
- 1–9 MAUDE reports citing this UDI
- No Linked premarket submission
- Yes 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: