FDA UDI In Commercial Distribution 🇺🇸 United States

Proliant Posterior Pedicle Screw & Hook System

DI: 00840996150477 · Model: 05-059-14-0000 · Choice Spine, LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Proliant Posterior Pedicle Screw & Hook System
Primary DI
00840996150477
Version / Model
05-059-14-0000
Company Name
Choice Spine, LP
Labeler DUNS
078293017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-06
Public Version
1
Public Version Date
2018-10-08
Public Version Status
New
Public Device Record Key
f3929642-2e61-4013-89f2-30d4ed260539

Device Description

PROLIANT, COUNTER TORQUE

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

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

Identifiers

Type ID
Primary 00840996150477

Customer Contacts