eudamed_udi
Primary ID: 08033860042905
STERNOBELL EXPLANT (UDI 08033860042905)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERNOBELL EXPLANT - Primary ID 08033860042905
Device Regulatory Overview
The STERNOBELL EXPLANT (Model/Catalog Number: RNE1325) is a medical device manufactured by BIOPSYBELL SRL. This product is indexed under FDA Product Code / Category Classification A01020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RNE1325
- Product Code / EMDN
- A01020202
- Device Name
- NEEDLES FOR BIOPSY OR EXPLANT
- Database Sync Date
- 2026-08-09 16:46:25
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 STERNOBELL EXPLANT?
The registered manufacturer of record for STERNOBELL EXPLANT is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for STERNOBELL EXPLANT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033860042905.
What classification code is assigned to this device?
This device is registered under product classification code A01020202.
Similar Classification Devices (A01020202)
Other Devices by BIOPSYBELL SRL
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