Giardia/Cryptosporidium Ag (stool) ELISA (UDI EIA-6059)
Manufactured by DRG Instruments Gesellschaft mit beschrnkter Haftung
Device Regulatory Overview
The Giardia/Cryptosporidium Ag (stool) ELISA (Model/Catalog Number: EIA-6059) is a medical device manufactured by DRG Instruments Gesellschaft mit beschrnkter Haftung. This product is indexed under FDA Product Code / Category Classification MHI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EIA-6059
- Product Code / EMDN
- MHI
- Device Name
- The Quantitative Determination of Total Thyroxine Concentration in Human Serum or Plasma by a Microplate Enzyme Immunoassay
- Database Sync Date
- 2026-08-09 09:12:11
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 Giardia/Cryptosporidium Ag (stool) ELISA?
The registered manufacturer of record for Giardia/Cryptosporidium Ag (stool) ELISA is DRG Instruments Gesellschaft mit beschrnkter Haftung.
What is the Primary UDI-DI identifier for Giardia/Cryptosporidium Ag (stool) ELISA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EIA-6059.
What classification code is assigned to this device?
This device is registered under product classification code MHI.
Similar Classification Devices (MHI)
Other Devices by DRG Instruments Gesellschaft mit beschrnkter Haftung
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