OVERHOLT GEISSENDOERFER Fig. 5 (UDI 04250379817396)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The OVERHOLT GEISSENDOERFER Fig. 5 (Model/Catalog Number: 12-4201-05) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L07080102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12-4201-05
- Product Code / EMDN
- L07080102
- Device Name
- Klemme, Arterie
- Database Sync Date
- 2026-08-09 16:29:12
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 OVERHOLT GEISSENDOERFER Fig. 5?
The registered manufacturer of record for OVERHOLT GEISSENDOERFER Fig. 5 is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for OVERHOLT GEISSENDOERFER Fig. 5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379817396.
What classification code is assigned to this device?
This device is registered under product classification code L07080102.
Similar Classification Devices (L07080102)
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