UDI device identifier
Adler Instrument Company 38-4985CC
UDI device identifier 00081022080089 · Adler, Inc.
Key facts
| Primary DI | 00081022080089 |
|---|---|
| Brand name | Adler Instrument Company |
| Version or model | 38-4985CC |
| Company | Adler, Inc. |
| DUNS number | 830141235 |
| Product code | HAE |
| GMDN term | Spinal rongeur |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 27, 2026 |
| Version date | May 14, 2026 |
| Description | Ejector Rongeur, Angled Up 40 degrees, TW 5mm, SL 200mm (8") Ceramic Coated |
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: