UDI device identifier
Meridian Medical 1002F
UDI device identifier 00081506704258 · Drive Devilbiss Healthcare
Key facts
| Primary DI | 00081506704258 |
|---|---|
| Brand name | Meridian Medical |
| Version or model | 1002F |
| Company | Drive Devilbiss Healthcare |
| DUNS number | 867673159 |
| Product code | FNM |
| GMDN term | Alternating-pressure bed mattress overlay, reusable |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 18, 2016 |
| Version date | May 27, 2026 |
| Description | APP PAD W/HEAD & FOOT FLAPS |
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: