gudid
Primary ID: 504
Otoform Kc (UDI 504)
Manufactured by Dreve Otoplastik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Otoform Kc - Primary ID 504
Device Regulatory Overview
The Otoform Kc (Model/Catalog Number: 504) is a medical device manufactured by Dreve Otoplastik GmbH. This product is indexed under FDA Product Code / Category Classification LDG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 504
- Product Code / EMDN
- LDG
- Device Name
- No.
- Database Sync Date
- 2026-08-09 09:07:32
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 Otoform Kc?
The registered manufacturer of record for Otoform Kc is Dreve Otoplastik GmbH.
What is the Primary UDI-DI identifier for Otoform Kc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 504.
What classification code is assigned to this device?
This device is registered under product classification code LDG.
Similar Classification Devices (LDG)
Other Devices by Dreve Otoplastik GmbH
Programmatic Export
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