WHITE Reiniger 8-k. Fig. 3 (UDI 04250379934635)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The WHITE Reiniger 8-k. Fig. 3 (Model/Catalog Number: 83-2601-03) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L159001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 83-2601-03
- Product Code / EMDN
- L159001
- Device Name
- Dental-Handinstrument
- Database Sync Date
- 2026-08-09 16:29:18
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 WHITE Reiniger 8-k. Fig. 3?
The registered manufacturer of record for WHITE Reiniger 8-k. Fig. 3 is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for WHITE Reiniger 8-k. Fig. 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379934635.
What classification code is assigned to this device?
This device is registered under product classification code L159001.
Similar Classification Devices (L159001)
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