gudid
Primary ID: 9106
Everyday (UDI 9106)
Manufactured by HOLLISTER INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Everyday - Primary ID 9106
Device Regulatory Overview
The Everyday (Model/Catalog Number: 9106) is a medical device manufactured by HOLLISTER INCORPORATED. This product is indexed under FDA Product Code / Category Classification NNX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9106
- Product Code / EMDN
- NNX
- Device Name
- Male Incontinence Catheter, Self-Adhesive
- Database Sync Date
- 2026-08-09 09:31:01
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Everyday?
The registered manufacturer of record for Everyday is HOLLISTER INCORPORATED.
What is the Primary UDI-DI identifier for Everyday?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9106.
What classification code is assigned to this device?
This device is registered under product classification code NNX.
Similar Classification Devices (NNX)
Other Devices by HOLLISTER INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint