UDI device identifier
maxill Safeguard Paper Sterilization Wrap - 24" x 24" Crepe Paper 60163
UDI device identifier 00060705601636 · MAXILL, INC.
Key facts
| Primary DI | 00060705601636 |
|---|---|
| Brand name | maxill Safeguard Paper Sterilization Wrap - 24" x 24" Crepe Paper |
| Version or model | 60163 |
| Company | MAXILL, INC. |
| DUNS number | 079343581 |
| Product code | FRG |
| GMDN term | Instrument/equipment drape, single-use, non-sterile |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 19, 2016 |
| Version date | Mar 29, 2018 |
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: