GUDIDData
gudid Primary ID: ART-8031

SAGE Vitrification Warming Kit (UDI ART-8031)

Manufactured by Coopersurgical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SAGE Vitrification Warming Kit - Primary ID ART-8031

Device Regulatory Overview

The SAGE Vitrification Warming Kit (Model/Catalog Number: ART-8031) is a medical device manufactured by Coopersurgical, Inc.. This product is indexed under FDA Product Code / Category Classification MQL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ART-8031
Product Code / EMDN
MQL
Device Name
SAGE Vitrification Warming Kit, ART-8031 (in plastic cryo vials): 2x2 ml of 1,0 M ART-8031-A Sucrose Warming Solution. 2x2 ml of 0,5 M ART-8031-B Sucrose Warming Solution. 2x2 ml of ART-8031-C MOPS Solution.
Database Sync Date
2026-08-09 09:16:47

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 SAGE Vitrification Warming Kit?

The registered manufacturer of record for SAGE Vitrification Warming Kit is Coopersurgical, Inc..

What is the Primary UDI-DI identifier for SAGE Vitrification Warming Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ART-8031.

What classification code is assigned to this device?

This device is registered under product classification code MQL.

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