UDI device identifier
Assure® Slide Pill Swallowing Aid forte 1000002
UDI device identifier 00015482100025 · Arkray USA, Inc.
Key facts
| Primary DI | 00015482100025 |
|---|---|
| Brand name | Assure® Slide Pill Swallowing Aid forte |
| Version or model | 1000002 |
| Company | Arkray USA, Inc. |
| DUNS number | 008171162 |
| Product code | NXB |
| GMDN term | Pill swallowing lubricant |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 28, 2018 |
| Version date | Aug 24, 2026 |
| Description | Assure Slide Pill Swallowing Aid is for people with swallowing difficulties, a gell that helps to swallow tablets, capsules and powders. (Primary UPC# 015482100025 is used as the assigned UDI for the Class I device.) |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: