FDA UDI In Commercial Distribution 🇺🇸 United States

Argo KnotlessTM

DI: 30653405988353 · Model: K4755RSP · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Argo KnotlessTM
Primary DI
30653405988353
Version / Model
K4755RSP
Catalog Number
K4755RSP
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-13
Public Version
1
Public Version Date
2023-01-23
Public Version Status
New
Public Device Record Key
1b3ac90a-7130-40f3-9a7a-10191f295416

Device Description

4.75/5.5 mm Argo KnotlessTM Reusable Smooth 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
No
Has Expiration Date
Yes
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
36167 Orthopaedic broach

Identifiers

Type ID
Direct Marking 10653405988359
Primary 30653405988353

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY