eudamed_udi
Primary ID: +E251195002991
bepro Suction Mixing Cup (UDI +E251195002991)
Manufactured by ALPRO MEDICAL GMBH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for bepro Suction Mixing Cup - Primary ID +E251195002991
Device Regulatory Overview
The bepro Suction Mixing Cup (Model/Catalog Number: 19500299) is a medical device manufactured by ALPRO MEDICAL GMBH. This product is indexed under FDA Product Code / Category Classification V80 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19500299
- Product Code / EMDN
- V80
- Device Name
- bepro Suction Mixing Cup
- Database Sync Date
- 2026-08-09 16:29:34
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 bepro Suction Mixing Cup?
The registered manufacturer of record for bepro Suction Mixing Cup is ALPRO MEDICAL GMBH.
What is the Primary UDI-DI identifier for bepro Suction Mixing Cup?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E251195002991.
What classification code is assigned to this device?
This device is registered under product classification code V80.
Similar Classification Devices (V80)
Other Devices by ALPRO MEDICAL GMBH
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