Vermed (UDI SHRPSHARPS 2Q/2L USA RED, SQUARE)
Manufactured by GRAPHIC CONTROLS ACQUISITION CORP
Device Regulatory Overview
The Vermed (Model/Catalog Number: SHRPSHARPS 2Q/2L USA 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
- SHRPSHARPS 2Q/2L USA RED, SQUARE
- Product Code / EMDN
- MMK
- Device Name
- SHRPSHARPS 2Q/2L USA RED, SQUARE
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 SHRPSHARPS 2Q/2L USA RED, SQUARE.
What classification code is assigned to this device?
This device is registered under product classification code MMK.
Similar Classification Devices (MMK)
Other Devices by GRAPHIC CONTROLS ACQUISITION CORP
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