ROCHESTER PEAN Arterienklemme (UDI 04250379816061)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The ROCHESTER PEAN Arterienklemme (Model/Catalog Number: 12-3101-14) 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
- 12-3101-14
- Product Code / EMDN
- L07080102
- Device Name
- Klemme, Arterie
- Database Sync Date
- 2026-08-09 16:29:06
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 ROCHESTER PEAN Arterienklemme?
The registered manufacturer of record for ROCHESTER PEAN Arterienklemme is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for ROCHESTER PEAN Arterienklemme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379816061.
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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