BENNETT Knochenhebel 65 mm 24 cm (UDI 04250379852144)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The BENNETT Knochenhebel 65 mm 24 cm (Model/Catalog Number: 32-7701-71) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L0902 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 32-7701-71
- Product Code / EMDN
- L0902
- Device Name
- Elevatorium, Orthopädie
- Database Sync Date
- 2026-08-09 16:28:52
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 BENNETT Knochenhebel 65 mm 24 cm?
The registered manufacturer of record for BENNETT Knochenhebel 65 mm 24 cm is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for BENNETT Knochenhebel 65 mm 24 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379852144.
What classification code is assigned to this device?
This device is registered under product classification code L0902.
Similar Classification Devices (L0902)
Other Devices by Zepf Medical Instruments GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint