eudamed_udi
Primary ID: 04262556375612
Unspecified Brand (UDI 04262556375612)
Manufactured by Remy & Geiser GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04262556375612
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 9855-AR240001) is a medical device manufactured by Remy & Geiser GmbH. This product is indexed under FDA Product Code / Category Classification A99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9855-AR240001
- Product Code / EMDN
- A99
- Device Name
- DROPPER ASSEMBLY
- Database Sync Date
- 2026-08-09 16:28:53
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Remy & Geiser GmbH.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262556375612.
What classification code is assigned to this device?
This device is registered under product classification code A99.
Similar Classification Devices (A99)
Other Devices by Remy & Geiser GmbH
Programmatic Export
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JSON API Endpoint