FDA UDI In Commercial Distribution 🇺🇸 United States

Argo Knotless

DI: 30845854083233 · Model: K4755RBP · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Argo Knotless
Primary DI
30845854083233
Version / Model
K4755RBP
Catalog Number
K4755RBP
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
2022-09-22
Public Version Status
Update
Public Device Record Key
f59f8aaf-4b42-4755-a5a8-a9860f50d195

Device Description

4.75/5.5mm Argo KnotlessTM Reusable Broaching Punch

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
No

Product Codes

Code Name
HWX TAP, BONE

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 30845854083233
Direct Marking 10845854083239

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY