GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: D-B1017-27E3

MicroScan Neg ID Panel Type 2 (UDI D-B1017-27E3)

Manufactured by Beckman Coulter Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MicroScan Neg ID Panel Type 2 - Primary ID D-B1017-27E3

Device Regulatory Overview

The MicroScan Neg ID Panel Type 2 (Model/Catalog Number: B1017-27) is a medical device manufactured by Beckman Coulter Inc.. This product is indexed under FDA Product Code / Category Classification W0203010185 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-0071-2026 View Full Alert →

SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-0441-2026 View Full Alert →

SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-0032-2026 View Full Alert →

DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clin...

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

Technical Specifications

Model Number
B1017-27
Product Code / EMDN
W0203010185
Device Name
MicroScan Neg ID Panel Type 2
Database Sync Date
2026-08-09 17:07:11

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of MicroScan Neg ID Panel Type 2?

The registered manufacturer of record for MicroScan Neg ID Panel Type 2 is Beckman Coulter Inc..

What is the Primary UDI-DI identifier for MicroScan Neg ID Panel Type 2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-B1017-27E3.

What classification code is assigned to this device?

This device is registered under product classification code W0203010185.

Similar Classification Devices (W0203010185)

Other Devices by Beckman Coulter Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint