UDI device identifier
Mui Scientific SPR1R(150)
UDI device identifier 00006784672921 · H & A Mui Enterprises Inc
Key facts
| Primary DI | 00006784672921 |
|---|---|
| Brand name | Mui Scientific |
| Version or model | SPR1R(150) |
| Company | H & A Mui Enterprises Inc |
| DUNS number | 243872611 |
| Product code | FFX |
| GMDN term | Gastrointestinal motility manometric catheter, non-electronic |
| Premarket submission | K823701 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 2, 2018 |
| Version date | Aug 5, 2022 |
| Description | Catheter Single-Use Anorectal Expulsion |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: