FDA UDI In Commercial Distribution 🇺🇸 United States

Binary

DI: M719GCP24680 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Binary
Primary DI
M719GCP24680
Version / Model
1
Catalog Number
GCP2-468
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
5c9a518a-e128-432d-a82d-da51aab3ff8d

Device Description

4-Level Binary Cervical Plate

Device Characteristics

Single Use
Yes
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary M719GCP24680

Customer Contacts

Phone
512-381-7070

Device Sizes

Type Value Unit Text
Length 68 Millimeter