eudamed_udi
Primary ID: 06971225933333
Apo B Control (UDI 06971225933333)
Manufactured by Goldsite Diagnostics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Apo B Control - Primary ID 06971225933333
Device Regulatory Overview
The Apo B Control (Model/Catalog Number: DM042) is a medical device manufactured by Goldsite Diagnostics Inc.. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DM042
- Product Code / EMDN
- W0102152003
- Device Name
- Apo B Control
- Database Sync Date
- 2026-08-09 16:29:15
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 Apo B Control?
The registered manufacturer of record for Apo B Control is Goldsite Diagnostics Inc..
What is the Primary UDI-DI identifier for Apo B Control?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971225933333.
What classification code is assigned to this device?
This device is registered under product classification code W0102152003.
Similar Classification Devices (W0102152003)
Other Devices by Goldsite Diagnostics Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint