Vermed (UDI SHRP12 GAL RCRA W/PORT/DUO LID)
Manufactured by GRAPHIC CONTROLS ACQUISITION CORP
Device Regulatory Overview
The Vermed (Model/Catalog Number: SHRP12 GAL RCRA W/PORT/DUO LID) 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
- SHRP12 GAL RCRA W/PORT/DUO LID
- Product Code / EMDN
- MMK
- Device Name
- SHRP12 GAL RCRA W/PORT/DUO LID
- 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 SHRP12 GAL RCRA W/PORT/DUO LID.
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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