FDA UDI In Commercial Distribution 🇺🇸 United States

TiLock

DI: M719GM1120 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TiLock
Primary DI
M719GM1120
Version / Model
1
Catalog Number
GM112
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
4
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
d6ba99b4-f87f-4204-8609-d32a175dfc8f

Device Description

Cortical Drill Guide

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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary M719GM1120

Customer Contacts

Phone
512-381-7070