gudid
Primary ID: 464
Otoform Ak (UDI 464)
Manufactured by Dreve Otoplastik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Otoform Ak - Primary ID 464
Device Regulatory Overview
The Otoform Ak (Model/Catalog Number: 464) 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
- 464
- 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 Ak?
The registered manufacturer of record for Otoform Ak is Dreve Otoplastik GmbH.
What is the Primary UDI-DI identifier for Otoform Ak?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 464.
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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