eudamed_udi
Primary ID: 07612334105424
MAXFRAME (UDI 07612334105424)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAXFRAME - Primary ID 07612334105424
Device Regulatory Overview
The MAXFRAME (Model/Catalog Number: 61.312.002) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification Z12011399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 61.312.002
- Product Code / EMDN
- Z12011399
- Device Name
- Cases for Trauma/ CMF Devices
- Database Sync Date
- 2026-08-09 16:29:13
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 MAXFRAME?
The registered manufacturer of record for MAXFRAME is Synthes GmbH.
What is the Primary UDI-DI identifier for MAXFRAME?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07612334105424.
What classification code is assigned to this device?
This device is registered under product classification code Z12011399.
Similar Classification Devices (Z12011399)
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