FDA UDI In Commercial Distribution 🇺🇸 United States

VitreQ

DI: 08719214222024 · Model: BF00.R02 · Vitreq B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VitreQ
Primary DI
08719214222024
Version / Model
BF00.R02
Company Name
Vitreq B.V.
Labeler DUNS
491393613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-21
Public Version
1
Public Version Date
2022-10-31
Public Version Status
New
Public Device Record Key
bb129da5-fb7f-465e-a1d2-9c97fd2d43d9

Device Description

Luer-lock Backflush Instrument with Passive and Active Aspiration

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
17899 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Identifiers

Type ID
Direct Marking 18719214222021
Primary 08719214222024

Customer Contacts