eudamed_udi
Primary ID: 04260114140863
ASTODIA (UDI 04260114140863)
Manufactured by Stihler Electronic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASTODIA - Primary ID 04260114140863
Device Regulatory Overview
The ASTODIA (Model/Catalog Number: DIA130) is a medical device manufactured by Stihler Electronic GmbH. This product is indexed under FDA Product Code / Category Classification Z110702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DIA130
- Product Code / EMDN
- Z110702
- Device Name
- ASTODIA
- Database Sync Date
- 2026-08-09 17:02:39
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 ASTODIA?
The registered manufacturer of record for ASTODIA is Stihler Electronic GmbH.
What is the Primary UDI-DI identifier for ASTODIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260114140863.
What classification code is assigned to this device?
This device is registered under product classification code Z110702.
Similar Classification Devices (Z110702)
Other Devices by Stihler Electronic GmbH
Programmatic Export
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