gudid
Primary ID: 1508047
ALTAPORE (UDI 1508047)
Manufactured by Apatech Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALTAPORE - Primary ID 1508047
Device Regulatory Overview
The ALTAPORE (Model/Catalog Number: 1508047) 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
- 1508047
- Product Code / EMDN
- MQV
- Device Name
- Bioactive and Osteoconductive - Silicate Substituted Calcium Phosphate bone void filler
- Database Sync Date
- 2026-08-09 09:08:43
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 ALTAPORE?
The registered manufacturer of record for ALTAPORE is Apatech Ltd.
What is the Primary UDI-DI identifier for ALTAPORE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1508047.
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
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