FDA UDI In Commercial Distribution 🇺🇸 United States

Argo Knotless

DI: 20845854649845 · Model: K4755DBP · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Argo Knotless
Primary DI
20845854649845
Version / Model
K4755DBP
Catalog Number
K4755DBP
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-25
Public Version
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
c6ddf631-a30a-46e3-b948-c1475a30e3f0

Device Description

4.75/5.5mm Argo KnotlessTM Disposable Broaching Punch

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
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
56708 Bone tap, single-use

Identifiers

Type ID
Primary 20845854649845

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4.75/5.5 MM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY