eudamed_udi
Primary ID: 07350084978041
NORDIC -LARGE-weiss (UDI 07350084978041)
Manufactured by Nordic activity AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NORDIC -LARGE-weiss - Primary ID 07350084978041
Device Regulatory Overview
The NORDIC -LARGE-weiss (Model/Catalog Number: 1-2503-V) is a medical device manufactured by Nordic activity AB. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1-2503-V
- Product Code / EMDN
- Y1803
- Device Name
- Overbed table NORDIC LARGE white with sideboard
- Database Sync Date
- 2026-08-09 16:46:54
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 NORDIC -LARGE-weiss?
The registered manufacturer of record for NORDIC -LARGE-weiss is Nordic activity AB.
What is the Primary UDI-DI identifier for NORDIC -LARGE-weiss?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350084978041.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
Other Devices by Nordic activity AB
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