UDI device identifier
Safetex 890076
UDI device identifier 00187207000238 · Andwin Scientific
Key facts
| Primary DI | 00187207000238 |
|---|---|
| Brand name | Safetex |
| Version or model | 890076 |
| Company | Andwin Scientific |
| DUNS number | 028449445 |
| Product code | HHT |
| GMDN term | Cervical cytology scraper, single-use |
| Premarket submission | K983428 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 1, 2017 |
| Version date | Jul 6, 2018 |
| Description | SCRAPER, PLASTIC 8" SAFETEX DOUBLE ENDED (100) |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: