gudid
Primary ID: 506005078078
Actifuse Flow (UDI 506005078078)
Manufactured by Apatech Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actifuse Flow - Primary ID 506005078078
Device Regulatory Overview
The Actifuse Flow (Model/Catalog Number: 506005078078) is a medical device manufactured by Apatech Ltd. This product is indexed under FDA Product Code / Category Classification MQV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 506005078078
- Product Code / EMDN
- MQV
- Device Name
- Bone Graft Substitute - Silicate Substituted Calcium Phosphate - 5.0ml pack size
- Database Sync Date
- 2026-08-09 09:08:08
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 Actifuse Flow?
The registered manufacturer of record for Actifuse Flow is Apatech Ltd.
What is the Primary UDI-DI identifier for Actifuse Flow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 506005078078.
What classification code is assigned to this device?
This device is registered under product classification code MQV.
Similar Classification Devices (MQV)
Other Devices by Apatech Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint