gudid
Primary ID: 219000-46
Allied Medical LLC (UDI 219000-46)
Manufactured by Allied Medical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Allied Medical LLC - Primary ID 219000-46
Device Regulatory Overview
The Allied Medical LLC (Model/Catalog Number: 219000-46) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 219000-46
- Product Code / EMDN
- KDQ
- Device Name
- Collection Bottle
- Database Sync Date
- 2026-08-09 09:00:33
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 Allied Medical LLC?
The registered manufacturer of record for Allied Medical LLC is Allied Medical, LLC.
What is the Primary UDI-DI identifier for Allied Medical LLC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 219000-46.
What classification code is assigned to this device?
This device is registered under product classification code KDQ.
Similar Classification Devices (KDQ)
Other Devices by Allied Medical, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint