FDA UDI In Commercial Distribution 🇺🇸 United States

Argo Knotless GENESYS

DI: 30653405988605 · Model: KBC475RSP · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Argo Knotless GENESYS
Primary DI
30653405988605
Version / Model
KBC475RSP
Catalog Number
KBC475RSP
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-12
Public Version
2
Public Version Date
2024-08-14
Public Version Status
Update
Public Device Record Key
46c17ace-551f-46c9-af8a-eb8c3c713c6a

Device Description

4.75 mm Argo Knotless GENESYS 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
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
64337 Bone-coring punch, reusable

Identifiers

Type ID
Direct Marking 10653405988601
Primary 30653405988605

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY;DO NOT CRUSH