FDA UDI In Commercial Distribution 🇺🇸 United States

Cortina

DI: 00841508106487 · Model: 31-90-006-20090804 · NEUROSTRUCTURES, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cortina
Primary DI
00841508106487
Version / Model
31-90-006-20090804
Company Name
NEUROSTRUCTURES, INC
Labeler DUNS
079391677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-11
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
117a7f1b-983b-4d84-909c-0b079df415ff

Device Description

Trials 20x9x8x4

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00841508106487

Customer Contacts

Phone
8003526103