UDI device identifier
Protexter 1
UDI device identifier 00068162000511 · ICP MEDICAL, LLC
Key facts
| Primary DI | 00068162000511 |
|---|---|
| Brand name | Protexter |
| Version or model | 1 |
| Catalog number | ICP-8150FC-XL |
| Company | ICP MEDICAL, LLC |
| DUNS number | 078780963 |
| Product code | OEA |
| GMDN term | Isolation gown, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 31, 2023 |
| Version date | Nov 8, 2023 |
| Description | Isolation gown, SMS, AAMI Level II, Yellow, Over the Head, Full Coverage, Thumb Loop with Elastic Wrist, 2XL |
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: