eudamed_udi
Primary ID: 07034950210052
Unspecified Brand (UDI 07034950210052)
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 07034950210052
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 21005) is a medical device manufactured by Norgesplaster AS. This product is indexed under FDA Product Code / Category Classification V0501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21005
- Product Code / EMDN
- V0501
- Device Name
- TF 6.3 - PP Class IIa - Reusable
- Database Sync Date
- 2026-08-09 17:04:55
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 07034950210052.
What classification code is assigned to this device?
This device is registered under product classification code V0501.
Similar Classification Devices (V0501)
Other Devices by Norgesplaster AS
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