gudid
Primary ID: 2882
KETO-DIASTIX (UDI 2882)
Manufactured by ASCENSIA DIABETES CARE US INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KETO-DIASTIX - Primary ID 2882
Device Regulatory Overview
The KETO-DIASTIX (Model/Catalog Number: 2882) is a medical device manufactured by ASCENSIA DIABETES CARE US INC.. This product is indexed under FDA Product Code / Category Classification JIL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2882
- Product Code / EMDN
- JIL
- Device Name
- Reagent Strips for Urinalysis: Ketone; Glucose
- Database Sync Date
- 2026-08-09 09:34:07
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 KETO-DIASTIX?
The registered manufacturer of record for KETO-DIASTIX is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for KETO-DIASTIX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2882.
What classification code is assigned to this device?
This device is registered under product classification code JIL.
Similar Classification Devices (JIL)
Other Devices by ASCENSIA DIABETES CARE US INC.
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