UDI device identifier
LHB Industries Ultra Flex Intermed
UDI device identifier 00009235421840 · The Lighthouse For The Blind
Key facts
| Primary DI | 00009235421840 |
|---|---|
| Brand name | LHB Industries |
| Version or model | Ultra Flex Intermed |
| Catalog number | 2204042 |
| Company | The Lighthouse For The Blind |
| DUNS number | 051731214 |
| Product code | KOA |
| GMDN term | Urinary incontinence penis sheath/port, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 1, 2021 |
| Version date | Jun 10, 2022 |
| Description | Male External Catheter, Intermediate 32mm, Non Latex |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: