AESKUSLIDES® ANA HEp-2 (UDI 04250289512626)
Manufactured by Aesku.Diagnostics GmbH & Co. KG
Device Regulatory Overview
The AESKUSLIDES® ANA HEp-2 (Model/Catalog Number: 51.180.BULK5) is a medical device manufactured by Aesku.Diagnostics GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification W0102100101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 51.180.BULK5
- Product Code / EMDN
- W0102100101
- Device Name
- AESKUSLIDES® ANA HEp-2
- Database Sync Date
- 2026-08-09 16:28:55
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 AESKUSLIDES® ANA HEp-2?
The registered manufacturer of record for AESKUSLIDES® ANA HEp-2 is Aesku.Diagnostics GmbH & Co. KG.
What is the Primary UDI-DI identifier for AESKUSLIDES® ANA HEp-2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250289512626.
What classification code is assigned to this device?
This device is registered under product classification code W0102100101.
Similar Classification Devices (W0102100101)
Other Devices by Aesku.Diagnostics GmbH & Co. KG
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