eudamed_udi
Primary ID: +E2510350191
KDM Impression-Clean (UDI +E2510350191)
Manufactured by ALPRO MEDICAL GMBH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KDM Impression-Clean - Primary ID +E2510350191
Device Regulatory Overview
The KDM Impression-Clean (Model/Catalog Number: 035019) is a medical device manufactured by ALPRO MEDICAL GMBH. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 035019
- Product Code / EMDN
- D99
- Device Name
- PrintoSept-ID
- Database Sync Date
- 2026-08-09 16:59:59
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 KDM Impression-Clean?
The registered manufacturer of record for KDM Impression-Clean is ALPRO MEDICAL GMBH.
What is the Primary UDI-DI identifier for KDM Impression-Clean?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E2510350191.
What classification code is assigned to this device?
This device is registered under product classification code D99.
Similar Classification Devices (D99)
Other Devices by ALPRO MEDICAL GMBH
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