eudamed_udi
Primary ID: 08055400890302
H401-UP-GLASS (UDI 08055400890302)
Manufactured by Okolab S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for H401-UP-GLASS - Primary ID 08055400890302
Device Regulatory Overview
The H401-UP-GLASS (Model/Catalog Number: H401-UP-GLASS) is a medical device manufactured by Okolab S.r.l.. This product is indexed under FDA Product Code / Category Classification Z120499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H401-UP-GLASS
- Product Code / EMDN
- Z120499
- Device Name
- THERMAL PLATES
- Database Sync Date
- 2026-08-09 16:46:17
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 H401-UP-GLASS?
The registered manufacturer of record for H401-UP-GLASS is Okolab S.r.l..
What is the Primary UDI-DI identifier for H401-UP-GLASS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055400890302.
What classification code is assigned to this device?
This device is registered under product classification code Z120499.
Similar Classification Devices (Z120499)
Other Devices by Okolab S.r.l.
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