gudid
Primary ID: 03-6055
JEDMED (UDI 03-6055)
Manufactured by JEDMED INSTRUMENT COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JEDMED - Primary ID 03-6055
Device Regulatory Overview
The JEDMED (Model/Catalog Number: 03-6055) is a medical device manufactured by JEDMED INSTRUMENT COMPANY. This product is indexed under FDA Product Code / Category Classification CBC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03-6055
- Product Code / EMDN
- CBC
- Device Name
- Option: Conversion Kit / Glass Trap
- Database Sync Date
- 2026-08-09 09:36:12
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 JEDMED?
The registered manufacturer of record for JEDMED is JEDMED INSTRUMENT COMPANY.
What is the Primary UDI-DI identifier for JEDMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03-6055.
What classification code is assigned to this device?
This device is registered under product classification code CBC.
Similar Classification Devices (CBC)
Other Devices by JEDMED INSTRUMENT COMPANY
Programmatic Export
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