GUDIDData
gudid Primary ID: B2495-6A

Thermo Scientific GlucoCrush (UDI B2495-6A)

Manufactured by Fisher Diagnostics

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Thermo Scientific GlucoCrush - Primary ID B2495-6A

Device Regulatory Overview

The Thermo Scientific GlucoCrush (Model/Catalog Number: B2495-6A) is a medical device manufactured by Fisher Diagnostics. This product is indexed under FDA Product Code / Category Classification MRV within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1503-2025 View Full Alert →

Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays....

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1502-2025 View Full Alert →

Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2762-2017 View Full Alert →

Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fish...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
B2495-6A
Product Code / EMDN
MRV
Device Name
Database Sync Date
2026-08-09 09:21:10

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 Thermo Scientific GlucoCrush?

The registered manufacturer of record for Thermo Scientific GlucoCrush is Fisher Diagnostics.

What is the Primary UDI-DI identifier for Thermo Scientific GlucoCrush?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B2495-6A.

What classification code is assigned to this device?

This device is registered under product classification code MRV.

Programmatic Export

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