eudamed_udi
Primary ID: 06118002221577
SOLOJEKT (UDI 06118002221577)
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 - Primary ID 06118002221577
Device Regulatory Overview
The SOLOJEKT (Model/Catalog Number: IT-03-26-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-03-26-LL
- Product Code / EMDN
- A020199
- Device Name
- HYPODERMIC SYRINGE
- Database Sync Date
- 2026-08-09 16:28:57
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?
The registered manufacturer of record for SOLOJEKT is I'M Medicare SARL.
What is the Primary UDI-DI identifier for SOLOJEKT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06118002221577.
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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