eudamed_udi
Primary ID: +G375IMC13115160D
Killian forceps (UDI +G375IMC13115160D)
Manufactured by Immane Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Killian forceps - Primary ID +G375IMC13115160D
Device Regulatory Overview
The Killian forceps (Model/Catalog Number: IMC1311516) is a medical device manufactured by Immane Corporation. This product is indexed under FDA Product Code / Category Classification L149099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IMC1311516
- Product Code / EMDN
- L149099
- Device Name
- Rhinology Instruments
- Database Sync Date
- 2026-08-09 16:30:02
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 Killian forceps?
The registered manufacturer of record for Killian forceps is Immane Corporation.
What is the Primary UDI-DI identifier for Killian forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G375IMC13115160D.
What classification code is assigned to this device?
This device is registered under product classification code L149099.
Similar Classification Devices (L149099)
Other Devices by Immane Corporation
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