eudamed_udi
Primary ID: 15017599001990
Action (UDI 15017599001990)
Manufactured by Naturelle Consumer Products
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Action - Primary ID 15017599001990
Device Regulatory Overview
The Action (Model/Catalog Number: 3013224) is a medical device manufactured by Naturelle Consumer Products. This product is indexed under FDA Product Code / Category Classification Z12019003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3013224
- Product Code / EMDN
- Z12019003
- Device Name
- Sterile Saline Wound Cleansing Wipe
- Database Sync Date
- 2026-08-09 16:45:37
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 Action?
The registered manufacturer of record for Action is Naturelle Consumer Products.
What is the Primary UDI-DI identifier for Action?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15017599001990.
What classification code is assigned to this device?
This device is registered under product classification code Z12019003.
Similar Classification Devices (Z12019003)
Other Devices by Naturelle Consumer Products
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