gudid
Primary ID: 03R7401
Acetaminophen Calibrator (UDI 03R7401)
Manufactured by Sekisui Diagnostics, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acetaminophen Calibrator - Primary ID 03R7401
Device Regulatory Overview
The Acetaminophen Calibrator (Model/Catalog Number: 03R7401) is a medical device manufactured by Sekisui Diagnostics, LLC. This product is indexed under FDA Product Code / Category Classification JIT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03R7401
- Product Code / EMDN
- JIT
- Device Name
- Database Sync Date
- 2026-08-09 09:50:05
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 Acetaminophen Calibrator?
The registered manufacturer of record for Acetaminophen Calibrator is Sekisui Diagnostics, LLC.
What is the Primary UDI-DI identifier for Acetaminophen Calibrator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03R7401.
What classification code is assigned to this device?
This device is registered under product classification code JIT.
Similar Classification Devices (JIT)
Other Devices by Sekisui Diagnostics, LLC
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