gudid
Primary ID: 73807
AUTION Diluent SED (UDI 73807)
Manufactured by ARKRAY USA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AUTION Diluent SED - Primary ID 73807
Device Regulatory Overview
The AUTION Diluent SED (Model/Catalog Number: 73807) is a medical device manufactured by ARKRAY USA, INC.. This product is indexed under FDA Product Code / Category Classification KQO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 73807
- Product Code / EMDN
- KQO
- Device Name
- Consumable for the identification and enumeration of WBC, RBC, Casts, Epithelial Cells, and Bacteria as well as flags for pathologic casts, yeast, crystal, small round cells, mucus, and sperm in urine sediment.
- Database Sync Date
- 2026-08-09 09:45:59
Full Regulatory Attributes
🔒 Token Gated
{
"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 AUTION Diluent SED?
The registered manufacturer of record for AUTION Diluent SED is ARKRAY USA, INC..
What is the Primary UDI-DI identifier for AUTION Diluent SED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 73807.
What classification code is assigned to this device?
This device is registered under product classification code KQO.
Similar Classification Devices (KQO)
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