GUDIDData
gudid Primary ID: SHRPCYTO 2Q/2L RED, SQUARE

Vermed (UDI SHRPCYTO 2Q/2L RED, SQUARE)

Manufactured by GRAPHIC CONTROLS ACQUISITION CORP

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vermed - Primary ID SHRPCYTO 2Q/2L RED, SQUARE

Device Regulatory Overview

The Vermed (Model/Catalog Number: SHRPCYTO 2Q/2L RED, SQUARE) is a medical device manufactured by GRAPHIC CONTROLS ACQUISITION CORP. This product is indexed under FDA Product Code / Category Classification MMK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SHRPCYTO 2Q/2L RED, SQUARE
Product Code / EMDN
MMK
Device Name
SHRPCYTO 2Q/2L RED, SQUARE
Database Sync Date
2026-08-09 09:00:34

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 Vermed?

The registered manufacturer of record for Vermed is GRAPHIC CONTROLS ACQUISITION CORP.

What is the Primary UDI-DI identifier for Vermed?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SHRPCYTO 2Q/2L RED, SQUARE.

What classification code is assigned to this device?

This device is registered under product classification code MMK.

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