FDA UDI In Commercial Distribution 🇺🇸 United States

VitreQ

DI: 88719214220910 · Model: BF25.D02 · Vitreq B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VitreQ
Primary DI
88719214220910
Version / Model
BF25.D02
Company Name
Vitreq B.V.
Labeler DUNS
491393613
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-05
Public Version
1
Public Version Date
2022-09-13
Public Version Status
New
Public Device Record Key
1bc4c7ee-ba5c-40e3-b55f-c95900c0bdfb

Device Description

25G Brush Backflush Instrument

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
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
47130 Vitrectomy fluid/gas handling handpiece/cannula

Identifiers

Type ID
Primary 88719214220910

Customer Contacts