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eudamed_udi Primary ID: 00816879023053

Probe Wash Solution (UDI 00816879023053)

Manufactured by Hycor Biomedical LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Probe Wash Solution - Primary ID 00816879023053

Device Regulatory Overview

The Probe Wash Solution (Model/Catalog Number: 63170) is a medical device manufactured by Hycor Biomedical LLC. This product is indexed under FDA Product Code / Category Classification W0201020185 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0224-2020 View Full Alert →

HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide solution, Part # 308051, sold separately or as a component contai...

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Technical Specifications

Model Number
63170
Product Code / EMDN
W0201020185
Device Name
NOVEOS® Immunoassay System Accessories
Database Sync Date
2026-08-09 16:30:09

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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Frequently Asked Questions

Who is the primary manufacturer of Probe Wash Solution?

The registered manufacturer of record for Probe Wash Solution is Hycor Biomedical LLC.

What is the Primary UDI-DI identifier for Probe Wash Solution?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816879023053.

What classification code is assigned to this device?

This device is registered under product classification code W0201020185.

Similar Classification Devices (W0201020185)

Other Devices by Hycor Biomedical LLC

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