FDA UDI In Commercial Distribution 🇺🇸 United States

V-Lance

DI: 00380659120015 · Model: 8065912001 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
V-Lance
Primary DI
00380659120015
Version / Model
8065912001
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-18
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
0bca637f-abc6-422c-8358-10c661c64726

Device Description

Ophthalmic Corneal/Scleral V-Lance Knife 20 Gauge [1.3mm]

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
Yes
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 10380659120012
Primary 00380659120015

Customer Contacts