eudamed_udi
Primary ID: +EOROCDS110P9538
Orotol plus (UDI +EOROCDS110P9538)
Manufactured by orochemie GmbH + Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Orotol plus - Primary ID +EOROCDS110P9538
Device Regulatory Overview
The Orotol plus (Model/Catalog Number: CDS110P9538) is a medical device manufactured by orochemie GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification D0901 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CDS110P9538
- Product Code / EMDN
- D0901
- Device Name
- Disinfectants for non-invasive medical devices - Suction System Disinfection
- Database Sync Date
- 2026-08-09 16:48:58
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 Orotol plus?
The registered manufacturer of record for Orotol plus is orochemie GmbH + Co. KG.
What is the Primary UDI-DI identifier for Orotol plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +EOROCDS110P9538.
What classification code is assigned to this device?
This device is registered under product classification code D0901.
Similar Classification Devices (D0901)
Other Devices by orochemie GmbH + Co. KG
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