eudamed_udi
Primary ID: 08683020072213
MULTIPLUS (UDI 08683020072213)
Manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MULTIPLUS - Primary ID 08683020072213
Device Regulatory Overview
The MULTIPLUS (Model/Catalog Number: AL UG31) is a medical device manufactured by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Z11040185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AL UG31
- Product Code / EMDN
- Z11040185
- Device Name
- Ultrasound Gel
- Database Sync Date
- 2026-08-09 16:48:30
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 MULTIPLUS?
The registered manufacturer of record for MULTIPLUS is ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ..
What is the Primary UDI-DI identifier for MULTIPLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683020072213.
What classification code is assigned to this device?
This device is registered under product classification code Z11040185.
Similar Classification Devices (Z11040185)
Other Devices by ALG İLAÇ SANAYİ TİCARET LTD. ŞTİ.
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