eudamed_udi
Primary ID: 08427734035344
ADNPRO (UDI 08427734035344)
Manufactured by Telic, S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ADNPRO - Primary ID 08427734035344
Device Regulatory Overview
The ADNPRO (Model/Catalog Number: 2018002) is a medical device manufactured by Telic, S.A.U.. This product is indexed under FDA Product Code / Category Classification Z11040185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2018002
- Product Code / EMDN
- Z11040185
- Device Name
- Ultrasound gels
- Database Sync Date
- 2026-08-09 16:46:47
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 ADNPRO?
The registered manufacturer of record for ADNPRO is Telic, S.A.U..
What is the Primary UDI-DI identifier for ADNPRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08427734035344.
What classification code is assigned to this device?
This device is registered under product classification code Z11040185.
Similar Classification Devices (Z11040185)
Other Devices by Telic, S.A.U.
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