gudid
Primary ID: 565
Impression pads (UDI 565)
Manufactured by Dreve Otoplastik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Impression pads - Primary ID 565
Device Regulatory Overview
The Impression pads (Model/Catalog Number: 565) 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
- 565
- 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 Impression pads?
The registered manufacturer of record for Impression pads is Dreve Otoplastik GmbH.
What is the Primary UDI-DI identifier for Impression pads?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 565.
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
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