eudamed_udi
Primary ID: 07090057570017
Integralift 230 (UDI 07090057570017)
Manufactured by Integra International AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Integralift 230 - Primary ID 07090057570017
Device Regulatory Overview
The Integralift 230 (Model/Catalog Number: Integralift 230) is a medical device manufactured by Integra International AS. This product is indexed under FDA Product Code / Category Classification V08050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Integralift 230
- Product Code / EMDN
- V08050302
- Device Name
- Integralift 230
- Database Sync Date
- 2026-08-09 16:48:49
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 Integralift 230?
The registered manufacturer of record for Integralift 230 is Integra International AS.
What is the Primary UDI-DI identifier for Integralift 230?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07090057570017.
What classification code is assigned to this device?
This device is registered under product classification code V08050302.
Similar Classification Devices (V08050302)
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