eudamed_udi
Primary ID: 05065026439000
Unspecified Brand (UDI 05065026439000)
Manufactured by Kirchner Brands Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 05065026439000
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 3oz) is a medical device manufactured by Kirchner Brands Inc. This product is indexed under FDA Product Code / Category Classification M04040101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3oz
- Product Code / EMDN
- M04040101
- Device Name
- Steri-Wash Aftercare Piercing Spray
- Database Sync Date
- 2026-08-09 16:50:53
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Kirchner Brands Inc.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05065026439000.
What classification code is assigned to this device?
This device is registered under product classification code M04040101.
Similar Classification Devices (M04040101)
Other Devices by Kirchner Brands Inc
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