FDA UDI In Commercial Distribution 🇺🇸 United States

iFusion

DI: 00858848006230 · Model: iFusion · OPTOVUE, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iFusion
Primary DI
00858848006230
Version / Model
iFusion
Catalog Number
700-48363-003
Company Name
OPTOVUE, INC.
Labeler DUNS
196500461
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
4
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
cfac0b4f-9572-457d-9950-c87ef904699b

Device Description

iVue NR for iFusion System w/ 120V Table

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OBO Tomography, Optical Coherence
HKI Camera, Ophthalmic, Ac-Powered

GMDN Terms

Code Name
10551 Ophthalmic fundus camera
58850 Ophthalmic spectral-domain optical coherence tomography system

Identifiers

Type ID
Primary 00858848006230

Customer Contacts

Phone
866-941-9240

Premarket Submissions

Submission Number Supplement Number
K130656 000