Norgesplaster Scanpor tape beige 5cm x 10m (UDI 07022750425318)
Manufactured by Orkla Wound Care AB
Device Regulatory Overview
The Norgesplaster Scanpor tape beige 5cm x 10m (Model/Catalog Number: 510001722) is a medical device manufactured by Orkla Wound Care AB. This product is indexed under FDA Product Code / Category Classification M0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 510001722
- Product Code / EMDN
- M0599
- Device Name
- TD 69
- Database Sync Date
- 2026-08-09 16:29:23
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 Norgesplaster Scanpor tape beige 5cm x 10m?
The registered manufacturer of record for Norgesplaster Scanpor tape beige 5cm x 10m is Orkla Wound Care AB.
What is the Primary UDI-DI identifier for Norgesplaster Scanpor tape beige 5cm x 10m?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07022750425318.
What classification code is assigned to this device?
This device is registered under product classification code M0599.
Similar Classification Devices (M0599)
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