gudid
Primary ID: 490517
PrepStain Syringing Pipettes (UDI 490517)
Manufactured by TRIPATH IMAGING, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PrepStain Syringing Pipettes - Primary ID 490517
Device Regulatory Overview
The PrepStain Syringing Pipettes (Model/Catalog Number: 490517) is a medical device manufactured by TRIPATH IMAGING, INC.. This product is indexed under FDA Product Code / Category Classification MKQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 490517
- Product Code / EMDN
- MKQ
- Device Name
- PrepStain Syringing Pipettes
- Database Sync Date
- 2026-08-09 09:59:28
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 PrepStain Syringing Pipettes?
The registered manufacturer of record for PrepStain Syringing Pipettes is TRIPATH IMAGING, INC..
What is the Primary UDI-DI identifier for PrepStain Syringing Pipettes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 490517.
What classification code is assigned to this device?
This device is registered under product classification code MKQ.
Similar Classification Devices (MKQ)
Other Devices by TRIPATH IMAGING, INC.
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