UDI device identifier
ENNOVATE SY909TS
UDI device identifier 00001010634001 · Aesculap AG
Key facts
| Primary DI | 00001010634001 |
|---|---|
| Brand name | ENNOVATE |
| Version or model | SY909TS |
| Catalog number | SY909TS |
| Company | Aesculap AG |
| DUNS number | 315018218 |
| Product code | NKB |
| GMDN term | Bone-screw internal spinal fixation system, sterile |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 30, 2019 |
| Version date | Jul 2, 2025 |
| Description | ENNOVATE MIS STRAIGHT ROD 5.5X90MM |
At a glance
- None MAUDE reports citing this UDI
- No 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: