UDI device identifier
Timeter 16394
UDI device identifier 00026072001646 · Allied Medical, LLC
Key facts
| Primary DI | 00026072001646 |
|---|---|
| Brand name | Timeter |
| Version or model | 16394 |
| Catalog number | T16394 |
| Company | Allied Medical, LLC |
| DUNS number | 119066872 |
| Product code | BYK |
| GMDN term | Oxygen administration tent, neonatal/paediatric |
| Premarket submission | K941547 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 30, 2015 |
| Version date | Oct 13, 2025 |
| Description | CAM 4, w/ PCS 414, 230 V / 50 Hz |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: