gudid
Primary ID: 900364
AQUALOC (UDI 900364)
Manufactured by Biomet Orthopedics, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AQUALOC - Primary ID 900364
Device Regulatory Overview
The AQUALOC (Model/Catalog Number: 900364) is a medical device manufactured by Biomet Orthopedics, LLC. This product is indexed under FDA Product Code / Category Classification GEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 900364
- Product Code / EMDN
- GEA
- Device Name
- Database Sync Date
- 2026-08-09 09:10:49
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 AQUALOC?
The registered manufacturer of record for AQUALOC is Biomet Orthopedics, LLC.
What is the Primary UDI-DI identifier for AQUALOC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 900364.
What classification code is assigned to this device?
This device is registered under product classification code GEA.
Similar Classification Devices (GEA)
Other Devices by Biomet Orthopedics, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint