FDA UDI Not in Commercial Distribution 🇺🇸 United States

CONCORDE

DI: 10705034219035 · Model: 287505113 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONCORDE
Primary DI
10705034219035
Version / Model
287505113
Catalog Number
287505113
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
f114e0c9-3569-43ce-b3ec-3ee10f5bce8c
Distribution End Date
2018-06-20

Device Description

CONCORDE SYSTEM TRIAL 5 DEGREES, 13mm

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
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 10705034219035

Customer Contacts