eudamed_udi
Primary ID: 50604724600598
Crystal Violet (500ml) (UDI 50604724600598)
Manufactured by Pro-Lab Diagnostics UK
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Crystal Violet (500ml) - Primary ID 50604724600598
Device Regulatory Overview
The Crystal Violet (500ml) (Model/Catalog Number: PL.7000) is a medical device manufactured by Pro-Lab Diagnostics UK. This product is indexed under FDA Product Code / Category Classification W0104010804 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PL.7000
- Product Code / EMDN
- W0104010804
- Device Name
- Gram Stains
- Database Sync Date
- 2026-08-09 16:28:54
Full Regulatory Attributes
đź”’ Token Gated
{
"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 Crystal Violet (500ml)?
The registered manufacturer of record for Crystal Violet (500ml) is Pro-Lab Diagnostics UK.
What is the Primary UDI-DI identifier for Crystal Violet (500ml)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50604724600598.
What classification code is assigned to this device?
This device is registered under product classification code W0104010804.
Similar Classification Devices (W0104010804)
Other Devices by Pro-Lab Diagnostics UK
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