UDI device identifier
General Biopsy Tray GUTS1000
UDI device identifier 00886333001590 · ARGON MEDICAL DEVICES, INC.
Key facts
| Primary DI | 00886333001590 |
|---|---|
| Brand name | General Biopsy Tray |
| Version or model | GUTS1000 |
| Catalog number | GUTS1000 |
| Company | ARGON MEDICAL DEVICES, INC. |
| DUNS number | 140727624 |
| Product code | KNW |
| GMDN term | Bone marrow biopsy needle, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 20, 2016 |
| Version date | May 11, 2026 |
| Description | General Biopsy Tray |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No 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: