eudamed_udi
Primary ID: 07332343300626
Stericlens (UDI 07332343300626)
Manufactured by Aurena Laboratories AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Stericlens - Primary ID 07332343300626
Device Regulatory Overview
The Stericlens (Model/Catalog Number: 301 396) is a medical device manufactured by Aurena Laboratories AB. This product is indexed under FDA Product Code / Category Classification M04040101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 301 396
- Product Code / EMDN
- M04040101
- Device Name
- Wound Wash
- Database Sync Date
- 2026-08-09 18:37:51
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 Stericlens?
The registered manufacturer of record for Stericlens is Aurena Laboratories AB.
What is the Primary UDI-DI identifier for Stericlens?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07332343300626.
What classification code is assigned to this device?
This device is registered under product classification code M04040101.
Similar Classification Devices (M04040101)
Other Devices by Aurena Laboratories AB
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