eudamed_udi
Primary ID: 06118002220198
SOLOJEKT AD (UDI 06118002220198)
Manufactured by I'M Medicare SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SOLOJEKT AD - Primary ID 06118002220198
Device Regulatory Overview
The SOLOJEKT AD (Model/Catalog Number: IT-02-18-LL) is a medical device manufactured by I'M Medicare SARL. This product is indexed under FDA Product Code / Category Classification A020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IT-02-18-LL
- Product Code / EMDN
- A020199
- Device Name
- AD/RUP SYRINGE WITH NEEDLE
- Database Sync Date
- 2026-08-09 16:28:54
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 SOLOJEKT AD?
The registered manufacturer of record for SOLOJEKT AD is I'M Medicare SARL.
What is the Primary UDI-DI identifier for SOLOJEKT AD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06118002220198.
What classification code is assigned to this device?
This device is registered under product classification code A020199.
Similar Classification Devices (A020199)
Other Devices by I'M Medicare SARL
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