eudamed_udi
Primary ID: 04051308001066
PLIF II (UDI 04051308001066)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PLIF II - Primary ID 04051308001066
Device Regulatory Overview
The PLIF II (Model/Catalog Number: 22912-112-10) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification P09070101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22912-112-10
- Product Code / EMDN
- P09070101
- Device Name
- PLIF
- Database Sync Date
- 2026-08-09 16:28:50
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 PLIF II?
The registered manufacturer of record for PLIF II is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for PLIF II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04051308001066.
What classification code is assigned to this device?
This device is registered under product classification code P09070101.
Similar Classification Devices (P09070101)
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