FDA UDI Not in Commercial Distribution 🇺🇸 United States

GENESYS MATRYX

DI: 10845854017125 · Model: 238035M5 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GENESYS MATRYX
Primary DI
10845854017125
Version / Model
238035M5
Catalog Number
238035M5
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
6a389391-97ad-4997-b503-97eaa371b8fe
Distribution End Date
2018-06-21

Device Description

GENESYS MATRYX 8.0 X 35 MM INTERFERENCE SCREW

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
45039 Bioabsorbable orthopaedic bone screw

Identifiers

Type ID
Primary 10845854017125

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 8 Millimeter
Length 35 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY
Type
Storage Environment Temperature
Temperature Range
– 104 Degrees Fahrenheit