gudid
Primary ID: 6000
Alpha (UDI 6000)
Manufactured by VITALOGRAPH (IRELAND) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alpha - Primary ID 6000
Device Regulatory Overview
The Alpha (Model/Catalog Number: 6000) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6000
- Product Code / EMDN
- BZG
- Device Name
- 65000
- Database Sync Date
- 2026-08-09 09:22:51
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 Alpha?
The registered manufacturer of record for Alpha is VITALOGRAPH (IRELAND) LIMITED.
What is the Primary UDI-DI identifier for Alpha?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6000.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Similar Classification Devices (BZG)
Other Devices by VITALOGRAPH (IRELAND) LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint