FDA UDI In Commercial Distribution 🇺🇸 United States

Cabo™

DI: 00841508102014 · Model: 98-1510 · NEUROSTRUCTURES, INC
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
Cabo™
Primary DI
00841508102014
Version / Model
98-1510
Company Name
NEUROSTRUCTURES, INC
Labeler DUNS
079391677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
e10418f6-9b36-4db3-91b3-a7baa154387a

Device Description

Drill Bits 10mm

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00841508102014

Customer Contacts

Phone
8003526103