FDA UDI Not in Commercial Distribution 🇺🇸 United States

Coral

DI: 10381780010197 · Model: 10-10-9580 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Coral
Primary DI
10381780010197
Version / Model
10-10-9580
Catalog Number
10-10-9580
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-18
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
4f51118f-1cd4-497d-affc-5fcc545fec60
Distribution End Date
2015-11-15

Device Description

Fixed Screw 9.50mm x 80mm

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
No
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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Secondary M248101095801
Primary 10381780010197

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9.50mm x 80mm