Vermed (UDI SHRP5.4 QT SHARPS WALL UNIT)
Manufactured by GRAPHIC CONTROLS ACQUISITION CORP
Device Regulatory Overview
The Vermed (Model/Catalog Number: SHRP5.4 QT SHARPS WALL UNIT) 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
- SHRP5.4 QT SHARPS WALL UNIT
- Product Code / EMDN
- MMK
- Device Name
- SHRP5.4 QT SHARPS WALL UNIT
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 SHRP5.4 QT SHARPS WALL UNIT.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint