gudid
Primary ID: T.9549.18
Gimmi (UDI T.9549.18)
Manufactured by Gimmi GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gimmi - Primary ID T.9549.18
Device Regulatory Overview
The Gimmi (Model/Catalog Number: T.9549.18) is a medical device manufactured by Gimmi GmbH. This product is indexed under FDA Product Code / Category Classification FJL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T.9549.18
- Product Code / EMDN
- FJL
- Device Name
- MONOPOLAR RESECTOSCOPE ELECTRODELOOP, ANGLED, FOR 30 SCOPE, SINGLE USEFOR 26 / 24 CH RESECTOSCOPE SHEATH
- Database Sync Date
- 2026-08-09 09:11:29
Full Regulatory Attributes
🔒 Token Gated
{
"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 Gimmi?
The registered manufacturer of record for Gimmi is Gimmi GmbH.
What is the Primary UDI-DI identifier for Gimmi?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is T.9549.18.
What classification code is assigned to this device?
This device is registered under product classification code FJL.
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