FDA UDI In Commercial Distribution 🇺🇸 United States

BIOPSYBELL

DI: 08033860046613 · Model: RENOVA SPINE KYPHOPLASTY TOOL KIT · BIOPSYBELL SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOPSYBELL
Primary DI
08033860046613
Version / Model
RENOVA SPINE KYPHOPLASTY TOOL KIT
Catalog Number
RESFAST11-003
Company Name
BIOPSYBELL SRL
Labeler DUNS
438746708
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-27
Public Version
1
Public Version Date
2025-11-04
Public Version Status
New
Public Device Record Key
159ae933-38b5-4340-8bd3-5c63014f3d20

Device Description

KYPHOPLASTY TOOL KIT

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCJ Spinal Channeling Instrument, Vertebroplasty

GMDN Terms

Code Name
58031 Bone access channel kit

Identifiers

Type ID
Primary 08033860046613

Customer Contacts

Phone
+39053527850

Device Sizes

Type Value Unit Text
Needle Gauge 10 Gauge