FDA UDI In Commercial Distribution 🇺🇸 United States

VitreQ

DI: 08719214222420 · Model: LP23.A05 · Vitreq B.V.
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VitreQ
Primary DI
08719214222420
Version / Model
LP23.A05
Company Name
Vitreq B.V.
Labeler DUNS
491393613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-12
Public Version
2
Public Version Date
2021-06-18
Public Version Status
Update
Public Device Record Key
069cf3ea-b801-486a-8f6c-86eb3bc71b9e

Device Description

23G (90°) Directional Illuminated Laser Probes, Alcon® Compatible

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
No
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
MPA Endoilluminator
HQF Laser, Ophthalmic
HQB Photocoagulator And Accessories

GMDN Terms

Code Name
61162 Ophthalmic laser system beam guide

Identifiers

Type ID
Package 08719214222413
Primary 08719214222420

Customer Contacts