UDI device identifier
First Aid Only 510-FR/REFILL
UDI device identifier 00092265510363 · Acme United Corporation
Key facts
| Primary DI | 00092265510363 |
|---|---|
| Brand name | First Aid Only |
| Version or model | 510-FR/REFILL |
| Catalog number | 510-FR/REFILL |
| Company | Acme United Corporation |
| DUNS number | 001180207 |
| Product code | LRR |
| GMDN term | First aid kit, medicated |
| Device class | Not classified |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 3, 2020 |
| Version date | Apr 15, 2021 |
| Description | First Responder Kit, Medium Refill Pack - Contains: Adhesive Plastic Bandages, 3/4" x 3" (32), Alcohol Pads (6), Biohazard Bag, 24" x 24" 10 gallon capacity, Burn Gel Packets, (3), Cold Pack, 4" x 5", CPR Face Shield, Emergency Blanket, 52" x 84", Eyewash - 4oz, First Aid Guide, Forceps, Hema-Seal… |
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: