eudamed_udi
Primary ID: 04066098422090
MULTILINE NEXT DC (UDI 04066098422090)
Manufactured by Greiner GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MULTILINE NEXT DC - Primary ID 04066098422090
Device Regulatory Overview
The MULTILINE NEXT DC (Model/Catalog Number: 4225200) is a medical device manufactured by Greiner GmbH. This product is indexed under FDA Product Code / Category Classification V08020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4225200
- Product Code / EMDN
- V08020101
- Device Name
- Multiline next DC
- 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 MULTILINE NEXT DC?
The registered manufacturer of record for MULTILINE NEXT DC is Greiner GmbH.
What is the Primary UDI-DI identifier for MULTILINE NEXT DC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04066098422090.
What classification code is assigned to this device?
This device is registered under product classification code V08020101.
Similar Classification Devices (V08020101)
Other Devices by Greiner GmbH
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