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Primary ID: P970018
PREPSTAIN (TM) SYSTEM (UDI P970018)
Manufactured by Bd Diagnostic Systems
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PREPSTAIN (TM) SYSTEM - Primary ID P970018
Device Regulatory Overview
The PREPSTAIN (TM) SYSTEM (Model/Catalog Number: Unspecified) is a medical device manufactured by Bd Diagnostic Systems. This product is indexed under FDA Product Code / Category Classification MKQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- MKQ
- Device Name
- Processor, cervical cytology slide, automated
- Database Sync Date
- 2026-08-09 10:05:00
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 (TM) SYSTEM?
The registered manufacturer of record for PREPSTAIN (TM) SYSTEM is Bd Diagnostic Systems.
What is the Primary UDI-DI identifier for PREPSTAIN (TM) SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P970018.
What classification code is assigned to this device?
This device is registered under product classification code MKQ.
Similar Classification Devices (MKQ)
Other Devices by Bd Diagnostic Systems
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