gudid
Primary ID: STERNOBELL
BIOPSYBELL SRL (UDI STERNOBELL)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIOPSYBELL SRL - Primary ID STERNOBELL
Device Regulatory Overview
The BIOPSYBELL SRL (Model/Catalog Number: STERNOBELL) is a medical device manufactured by BIOPSYBELL SRL. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- STERNOBELL
- Product Code / EMDN
- FCG
- Device Name
- Needle for bone-marrow biopsy
- Database Sync Date
- 2026-08-09 09:04:33
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 BIOPSYBELL SRL?
The registered manufacturer of record for BIOPSYBELL SRL is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for BIOPSYBELL SRL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is STERNOBELL.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by BIOPSYBELL SRL
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