eudamed_udi
Primary ID: 01220000220171
Unspecified Brand (UDI 01220000220171)
Manufactured by Fridababy, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 01220000220171
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: C-Section Silicone Scar Patches) is a medical device manufactured by Fridababy, LLC. This product is indexed under FDA Product Code / Category Classification M03030202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C-Section Silicone Scar Patches
- Product Code / EMDN
- M03030202
- Device Name
- C-Section Silicone Scar Patches
- Database Sync Date
- 2026-08-09 16:46:55
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 Fridababy, LLC.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01220000220171.
What classification code is assigned to this device?
This device is registered under product classification code M03030202.
Similar Classification Devices (M03030202)
Other Devices by Fridababy, LLC
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