UDI device identifier
Single Use Guide Sheath Kit K-203
UDI device identifier 04953170245503 · OLYMPUS MEDICAL SYSTEMS CORP.
Key facts
| Primary DI | 04953170245503 |
|---|---|
| Brand name | Single Use Guide Sheath Kit |
| Version or model | K-203 |
| Company | OLYMPUS MEDICAL SYSTEMS CORP. |
| DUNS number | 711789789 |
| Product code | EOQ |
| GMDN term | Flexible endoscopic biopsy forceps, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 21, 2018 |
| Version date | Apr 1, 2024 |
| Description | Single Use Guide Sheath Kit |
At a glance
- 1–9 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: