eudamed_udi
Primary ID: 08033860026929
DISKOM (UDI 08033860026929)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DISKOM - Primary ID 08033860026929
Device Regulatory Overview
The DISKOM (Model/Catalog Number: DKR1908-SPA) is a medical device manufactured by BIOPSYBELL SRL. This product is indexed under FDA Product Code / Category Classification A01020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DKR1908-SPA
- Product Code / EMDN
- A01020102
- Device Name
- DISKOM
- Database Sync Date
- 2026-08-09 16:29:04
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 DISKOM?
The registered manufacturer of record for DISKOM is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for DISKOM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033860026929.
What classification code is assigned to this device?
This device is registered under product classification code A01020102.
Similar Classification Devices (A01020102)
Other Devices by BIOPSYBELL SRL
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