gudid
Primary ID: 03.52.10.0469
Spine Instruments (UDI 03.52.10.0469)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spine Instruments - Primary ID 03.52.10.0469
Device Regulatory Overview
The Spine Instruments (Model/Catalog Number: 03.52.10.0469) is a medical device manufactured by BIOPSYBELL SRL. This product is indexed under FDA Product Code / Category Classification GDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03.52.10.0469
- Product Code / EMDN
- GDF
- Device Name
- Kyphoplasty kirschner guide
- Database Sync Date
- 2026-08-09 09:04:34
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 Spine Instruments?
The registered manufacturer of record for Spine Instruments is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for Spine Instruments?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03.52.10.0469.
What classification code is assigned to this device?
This device is registered under product classification code GDF.
Similar Classification Devices (GDF)
Other Devices by BIOPSYBELL SRL
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