FDA UDI In Commercial Distribution 🇺🇸 United States

Windsor Knife

DI: 05060510711754 · Model: WK20GBU · CORE SURGICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Windsor Knife
Primary DI
05060510711754
Version / Model
WK20GBU
Catalog Number
WK20GBU
Company Name
CORE SURGICAL LIMITED
Labeler DUNS
236541301
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-01
Public Version
1
Public Version Date
2024-04-09
Public Version Status
New
Public Device Record Key
045a62ba-930c-403e-a692-3c675acb9f06

Device Description

Windsor Slit Knife/ Keratome 20 gauge angled sideport. Single bevel up full handle. Sterile. Single use

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
HNN Knife, Ophthalmic

GMDN Terms

Code Name
46741 Ophthalmic knife, single-use

Identifiers

Type ID
Package 15060510711751
Primary 05060510711754