GUDIDData
gudid Primary ID: N/A

GR01 HbA1c Elution Buffer No. 2 (UDI N/A)

Manufactured by TOSOH CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GR01 HbA1c Elution Buffer No. 2 - Primary ID N/A

Device Regulatory Overview

The GR01 HbA1c Elution Buffer No. 2 (Model/Catalog Number: N/A) is a medical device manufactured by TOSOH CORPORATION. This product is indexed under FDA Product Code / Category Classification LCP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
N/A
Product Code / EMDN
LCP
Device Name
Database Sync Date
2026-08-09 09:15:39

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 GR01 HbA1c Elution Buffer No. 2?

The registered manufacturer of record for GR01 HbA1c Elution Buffer No. 2 is TOSOH CORPORATION.

What is the Primary UDI-DI identifier for GR01 HbA1c Elution Buffer No. 2?

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

What classification code is assigned to this device?

This device is registered under product classification code LCP.

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