FDA UDI In Commercial Distribution 🇺🇸 United States

ULTRAFIX

DI: 10845854024195 · Model: 10121 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ULTRAFIX
Primary DI
10845854024195
Version / Model
10121
Catalog Number
10121
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2022-09-28
Public Version Status
Update
Public Device Record Key
ac0c33f0-72f8-49d3-8182-9b1919ad3af0

Device Description

ULTRAFIX ARTHROSCOPIC INSERTER

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
Yes
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
32865 Orthopaedic implant driver

Identifiers

Type ID
Direct Marking 20845854024192
Primary 10845854024195

Customer Contacts