UDI device identifier
MicroMyst 205000DS
UDI device identifier 10381780000112 · Integra Lifesciences Corporation
Key facts
| Primary DI | 10381780000112 |
|---|---|
| Brand name | MicroMyst |
| Version or model | 205000DS |
| Catalog number | 205000DS |
| Company | Integra Lifesciences Corporation |
| DUNS number | 083171244 |
| Product code | FMF |
| GMDN term | Open-surgery adhesive/sealant applicator, dual-channel |
| Premarket submission | K082454 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 29, 2016 |
| Version date | May 15, 2023 |
| Description | MicroMyst Applicator (14cm) 5 pack - for use with Flow Regulator |
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: