eudamed_udi
Primary ID: +E25131061
AlproJet-W 1 L (UDI +E25131061)
Manufactured by ALPRO MEDICAL GMBH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AlproJet-W 1 L - Primary ID +E25131061
Device Regulatory Overview
The AlproJet-W 1 L (Model/Catalog Number: 3106) is a medical device manufactured by ALPRO MEDICAL GMBH. This product is indexed under FDA Product Code / Category Classification V0799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3106
- Product Code / EMDN
- V0799
- Device Name
- AlproJet-W
- Database Sync Date
- 2026-08-09 16:29:11
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 AlproJet-W 1 L?
The registered manufacturer of record for AlproJet-W 1 L is ALPRO MEDICAL GMBH.
What is the Primary UDI-DI identifier for AlproJet-W 1 L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E25131061.
What classification code is assigned to this device?
This device is registered under product classification code V0799.
Similar Classification Devices (V0799)
Other Devices by ALPRO MEDICAL GMBH
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