MICROSCOPE KP PLUS PRINTER SLIDES (UDI 07312052930253)
Manufactured by VWR International B.V.
Device Regulatory Overview
The MICROSCOPE KP PLUS PRINTER SLIDES (Model/Catalog Number: PR-P-001) is a medical device manufactured by VWR International B.V.. This product is indexed under FDA Product Code / Category Classification W0503900201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PR-P-001
- Product Code / EMDN
- W0503900201
- Device Name
- Klinipath Slide
- Database Sync Date
- 2026-08-09 16:29:21
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 MICROSCOPE KP PLUS PRINTER SLIDES?
The registered manufacturer of record for MICROSCOPE KP PLUS PRINTER SLIDES is VWR International B.V..
What is the Primary UDI-DI identifier for MICROSCOPE KP PLUS PRINTER SLIDES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312052930253.
What classification code is assigned to this device?
This device is registered under product classification code W0503900201.
Similar Classification Devices (W0503900201)
Other Devices by VWR International B.V.
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