eudamed_udi
Primary ID: 03760246601160
SoftFil® Precision (UDI 03760246601160)
Manufactured by SOFT MEDICAL AESTHETICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SoftFil® Precision - Primary ID 03760246601160
Device Regulatory Overview
The SoftFil® Precision (Model/Catalog Number: CP2090/XL) is a medical device manufactured by SOFT MEDICAL AESTHETICS. This product is indexed under FDA Product Code / Category Classification A01010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CP2090/XL
- Product Code / EMDN
- A01010199
- Device Name
- CP2090/XL
- Database Sync Date
- 2026-08-09 16:28:44
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 SoftFil® Precision?
The registered manufacturer of record for SoftFil® Precision is SOFT MEDICAL AESTHETICS.
What is the Primary UDI-DI identifier for SoftFil® Precision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760246601160.
What classification code is assigned to this device?
This device is registered under product classification code A01010199.
Similar Classification Devices (A01010199)
Other Devices by SOFT MEDICAL AESTHETICS
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