FDA UDI In Commercial Distribution 🇺🇸 United States

BIOPSYBELL

DI: 08033860026004 · Model: DISKOM · BIOPSYBELL SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
BIOPSYBELL
Primary DI
08033860026004
Version / Model
DISKOM
Catalog Number
DKR1716BCD
Company Name
BIOPSYBELL SRL
Labeler DUNS
438746708
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-16
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
fab964da-a37a-4ecc-aef0-5cf0b85c518c

Device Description

DISC DECOMPRESSION NEEDLE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRX Arthroscope

GMDN Terms

Code Name
36077 Diskectomy system, percutaneous, automatic

Identifiers

Type ID
Primary 08033860026004

Customer Contacts

Phone
+39053527850

Premarket Submissions

Submission Number Supplement Number
K180315 000

Device Sizes

Type Value Unit Text
Length 160 Millimeter
Needle Gauge 17 Gauge