gudid
Primary ID: CKMB-6.5
JAS Diagnostics (UDI CKMB-6.5)
Manufactured by DREW SCIENTIFIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JAS Diagnostics - Primary ID CKMB-6.5
Device Regulatory Overview
The JAS Diagnostics (Model/Catalog Number: CKMB-6.5) is a medical device manufactured by DREW SCIENTIFIC, INC.. This product is indexed under FDA Product Code / Category Classification JHW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CKMB-6.5
- Product Code / EMDN
- JHW
- Device Name
- CK MB ISOENZYME REAGENT (10x 6.5mL)
- Database Sync Date
- 2026-08-09 09:31:21
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 JAS Diagnostics?
The registered manufacturer of record for JAS Diagnostics is DREW SCIENTIFIC, INC..
What is the Primary UDI-DI identifier for JAS Diagnostics?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CKMB-6.5.
What classification code is assigned to this device?
This device is registered under product classification code JHW.
Similar Classification Devices (JHW)
Other Devices by DREW SCIENTIFIC, INC.
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