gudid
Primary ID: CIFOPACK KIRSCHNER GUIDE
BIOPSYBELL (UDI CIFOPACK KIRSCHNER GUIDE)
Manufactured by BIOPSYBELL SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIOPSYBELL - Primary ID CIFOPACK KIRSCHNER GUIDE
Device Regulatory Overview
The BIOPSYBELL (Model/Catalog Number: CIFOPACK KIRSCHNER GUIDE) 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
- CIFOPACK KIRSCHNER GUIDE
- 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 BIOPSYBELL?
The registered manufacturer of record for BIOPSYBELL is BIOPSYBELL SRL.
What is the Primary UDI-DI identifier for BIOPSYBELL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CIFOPACK KIRSCHNER GUIDE.
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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