gudid
Primary ID: 6070591216
LUMAX REPLACEMENT HEAD (UDI 6070591216)
Manufactured by MAXILL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LUMAX REPLACEMENT HEAD - Primary ID 6070591216
Device Regulatory Overview
The LUMAX REPLACEMENT HEAD (Model/Catalog Number: 6070591216) is a medical device manufactured by MAXILL, INC.. This product is indexed under FDA Product Code / Category Classification EBZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6070591216
- Product Code / EMDN
- EBZ
- Device Name
- Database Sync Date
- 2026-08-09 09:03:34
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 LUMAX REPLACEMENT HEAD?
The registered manufacturer of record for LUMAX REPLACEMENT HEAD is MAXILL, INC..
What is the Primary UDI-DI identifier for LUMAX REPLACEMENT HEAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6070591216.
What classification code is assigned to this device?
This device is registered under product classification code EBZ.
Similar Classification Devices (EBZ)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint