FDA UDI In Commercial Distribution 🇺🇸 United States

Y-Knot

DI: 30845854021648 · Model: Y-PERC · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Y-Knot
Primary DI
30845854021648
Version / Model
Y-PERC
Catalog Number
Y-PERC
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-10
Public Version
1
Public Version Date
2021-05-18
Public Version Status
New
Public Device Record Key
c08085a1-a015-4e2c-9721-c886a6c3e5a5

Device Description

Y-Knot Flex Disposable Percutaneous Pack For Y-G00X Reusable Guides

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
No

Product Codes

Code Name
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
44093 Arthroscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 30845854021648

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY