eudamed_udi
Primary ID: 04056807546995
Unspecified Brand (UDI 04056807546995)
Manufactured by Norgesplaster AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04056807546995
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 12254) is a medical device manufactured by Norgesplaster AS. This product is indexed under FDA Product Code / Category Classification M0303010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12254
- Product Code / EMDN
- M0303010203
- Device Name
- TF 1.10 Soft/UNI
- Database Sync Date
- 2026-08-09 18:23:45
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Norgesplaster AS.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056807546995.
What classification code is assigned to this device?
This device is registered under product classification code M0303010203.
Similar Classification Devices (M0303010203)
Other Devices by Norgesplaster AS
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