eudamed_udi
Primary ID: 08033860042813
SPEEDYBELL DOPPIA CORSA & INTRODUTTORE (UDI 08033860042813)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPEEDYBELL DOPPIA CORSA & INTRODUTTORE - Primary ID 08033860042813
Device Regulatory Overview
The SPEEDYBELL DOPPIA CORSA & INTRODUTTORE (Model/Catalog Number: SBDTR2025EC) is a medical device manufactured by BIOPSYBELL SRL. This product is indexed under FDA Product Code / Category Classification A0102010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SBDTR2025EC
- Product Code / EMDN
- A0102010101
- Device Name
- NEEDLES FOR BIOPSY OR EXPLANT
- Database Sync Date
- 2026-08-09 16:28:44
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 SPEEDYBELL DOPPIA CORSA & INTRODUTTORE?
The registered manufacturer of record for SPEEDYBELL DOPPIA CORSA & INTRODUTTORE is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for SPEEDYBELL DOPPIA CORSA & INTRODUTTORE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033860042813.
What classification code is assigned to this device?
This device is registered under product classification code A0102010101.
Similar Classification Devices (A0102010101)
Other Devices by BIOPSYBELL SRL
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