UDI device identifier
TactiFlex™ Sensor Enabled™ A-TFSE-D
UDI device identifier 05415067034656 · ST. JUDE MEDICAL, INC.
Key facts
| Primary DI | 05415067034656 |
|---|---|
| Brand name | TactiFlex™ Sensor Enabled™ |
| Version or model | A-TFSE-D |
| Catalog number | A-TFSE-D |
| Company | ST. JUDE MEDICAL, INC. |
| DUNS number | 149818952 |
| Product code | OAE |
| GMDN term | Cardiac radio-frequency ablation system catheter |
| Premarket submission | P220013 |
| Device class | Class III |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | May 31, 2023 |
| Version date | Sep 9, 2025 |
| Description | Ablation Catheter |
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: