gudid
Primary ID: 73811
AUTION Sheath Solution (UDI 73811)
Manufactured by ARKRAY USA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AUTION Sheath Solution - Primary ID 73811
Device Regulatory Overview
The AUTION Sheath Solution (Model/Catalog Number: 73811) 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
- 73811
- 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 Sheath Solution?
The registered manufacturer of record for AUTION Sheath Solution is ARKRAY USA, INC..
What is the Primary UDI-DI identifier for AUTION Sheath Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 73811.
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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