gudid
Primary ID: 506005078064
Actifuse Shape (UDI 506005078064)
Manufactured by Apatech Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actifuse Shape - Primary ID 506005078064
Device Regulatory Overview
The Actifuse Shape (Model/Catalog Number: 506005078064) is a medical device manufactured by Apatech Ltd. This product is indexed under FDA Product Code / Category Classification LYC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 506005078064
- Product Code / EMDN
- LYC
- Device Name
- Bone Graft Substitute - Silicate Substituted Calcium Phosphate - 2.6ml pack size
- Database Sync Date
- 2026-08-09 09:08:08
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Actifuse Shape?
The registered manufacturer of record for Actifuse Shape is Apatech Ltd.
What is the Primary UDI-DI identifier for Actifuse Shape?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 506005078064.
What classification code is assigned to this device?
This device is registered under product classification code LYC.
Similar Classification Devices (LYC)
Other Devices by Apatech Ltd
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