GUDIDData
eudamed_udi Primary ID: 00816085023328

XPR-PLUS® Neutralizing Buffer (UDI 00816085023328)

Manufactured by CalibreScientific US, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XPR-PLUS® Neutralizing Buffer - Primary ID 00816085023328

Device Regulatory Overview

The XPR-PLUS® Neutralizing Buffer (Model/Catalog Number: 0003482) is a medical device manufactured by CalibreScientific US, Inc.. This product is indexed under FDA Product Code / Category Classification W010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0003482
Product Code / EMDN
W010499
Device Name
Digestion and Decontamination Reagents
Database Sync Date
2026-08-09 17:10:37

Full Regulatory Attributes

🔒 Token Gated
{
    "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 XPR-PLUS® Neutralizing Buffer?

The registered manufacturer of record for XPR-PLUS® Neutralizing Buffer is CalibreScientific US, Inc..

What is the Primary UDI-DI identifier for XPR-PLUS® Neutralizing Buffer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816085023328.

What classification code is assigned to this device?

This device is registered under product classification code W010499.

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