FDA UDI In Commercial Distribution 🇺🇸 United States

I² Kit for intraocular injection

DI: B384VS05201 · Model: VS0520 · Vortex Surgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
I² Kit for intraocular injection
Primary DI
B384VS05201
Version / Model
VS0520
Catalog Number
VS0520
Company Name
Vortex Surgical, Inc.
Labeler DUNS
080375891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-07
Public Version
4
Public Version Date
2022-11-21
Public Version Status
Update
Public Device Record Key
90f27c0b-8a7e-4a5d-8af8-d9adb8d1b31f

Device Description

Intraocular injection kit - standard set with drape (speculum, marker, drape, 18ga needle, 27ga needle, 30ga needle, gloves, swabs, 1.0 ml syringe)

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
No
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
45150 Ophthalmic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary B384VS05201

Customer Contacts

Phone
636-778-4350