UDI device identifier
BioZorb F0202
UDI device identifier 15420045513983 · Hologic, Inc.
Key facts
| Primary DI | 15420045513983 |
|---|---|
| Brand name | BioZorb |
| Version or model | F0202 |
| Catalog number | F0202 |
| Company | Hologic, Inc. |
| DUNS number | 018925968 |
| Product code | NEU |
| GMDN term | Radiological image marker, implantable |
| Premarket submission | K143484 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Apr 21, 2021 |
| Version date | Sep 4, 2026 |
| Description | BioZorb Marker |
At a glance
- 10–99 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: