eudamed_udi
Primary ID: 07332343300725
TW1000 EHS Eye + Wound Wash (UDI 07332343300725)
Manufactured by Aurena Laboratories AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TW1000 EHS Eye + Wound Wash - Primary ID 07332343300725
Device Regulatory Overview
The TW1000 EHS Eye + Wound Wash (Model/Catalog Number: 301428) 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
- 301428
- Product Code / EMDN
- M04040101
- Device Name
- Wound and Eye Wash Spray
- Database Sync Date
- 2026-08-09 16:59:11
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 TW1000 EHS Eye + Wound Wash?
The registered manufacturer of record for TW1000 EHS Eye + Wound Wash is Aurena Laboratories AB.
What is the Primary UDI-DI identifier for TW1000 EHS Eye + Wound Wash?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07332343300725.
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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