Presto® WOUND AND EYE RINSE SPRAY (UDI 07332343301265)
Manufactured by Aurena Laboratories AB
Device Regulatory Overview
The Presto® WOUND AND EYE RINSE SPRAY (Model/Catalog Number: 301515) 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
- 301515
- Product Code / EMDN
- M04040101
- Device Name
- Wound and Eye Wash Spray
- Database Sync Date
- 2026-08-09 16:50:32
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 Presto® WOUND AND EYE RINSE SPRAY?
The registered manufacturer of record for Presto® WOUND AND EYE RINSE SPRAY is Aurena Laboratories AB.
What is the Primary UDI-DI identifier for Presto® WOUND AND EYE RINSE SPRAY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07332343301265.
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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