eudamed_udi
Primary ID: 04710810117541
LF2 Nebulizer (UDI 04710810117541)
Manufactured by GaleMed Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LF2 Nebulizer - Primary ID 04710810117541
Device Regulatory Overview
The LF2 Nebulizer (Model/Catalog Number: AD0017) is a medical device manufactured by GaleMed Corporation. This product is indexed under FDA Product Code / Category Classification R03010304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AD0017
- Product Code / EMDN
- R03010304
- Device Name
- Nebulizer
- Database Sync Date
- 2026-08-09 17:14:15
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 LF2 Nebulizer?
The registered manufacturer of record for LF2 Nebulizer is GaleMed Corporation.
What is the Primary UDI-DI identifier for LF2 Nebulizer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710810117541.
What classification code is assigned to this device?
This device is registered under product classification code R03010304.
Similar Classification Devices (R03010304)
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