gudid
Primary ID: 66079659
Venus (UDI 66079659)
Manufactured by Kulzer GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Venus - Primary ID 66079659
Device Regulatory Overview
The Venus (Model/Catalog Number: 66079659) is a medical device manufactured by Kulzer GmbH. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 66079659
- Product Code / EMDN
- EFT
- Device Name
- Venus Rapid Fresh Cleanser 2 ct. sample
- Database Sync Date
- 2026-08-09 09:09:38
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 Venus?
The registered manufacturer of record for Venus is Kulzer GmbH.
What is the Primary UDI-DI identifier for Venus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66079659.
What classification code is assigned to this device?
This device is registered under product classification code EFT.
Similar Classification Devices (EFT)
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