gudid
Primary ID: CP1870/XL
SoftFil Precision (UDI CP1870/XL)
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 CP1870/XL
Device Regulatory Overview
The SoftFil Precision (Model/Catalog Number: CP1870/XL) is a medical device manufactured by SOFT MEDICAL AESTHETICS. This product is indexed under FDA Product Code / Category Classification GEA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CP1870/XL
- Product Code / EMDN
- GEA
- Device Name
- SoftFil Precision are sterile and single use injection kits containing: - 1 stainless steel pre-hole needle in its protective cap, - 1 stainless steel, graduated blunt-tip needle (micro-cannula) 18G x 70 mm in its protective cap.
- Database Sync Date
- 2026-08-09 09:33:50
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 CP1870/XL.
What classification code is assigned to this device?
This device is registered under product classification code GEA.
Similar Classification Devices (GEA)
Other Devices by SOFT MEDICAL AESTHETICS
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