FDA UDI In Commercial Distribution 🇺🇸 United States

imovifa

DI: 04573277310111 · Model: imovifa · CREWT MEDICAL SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
imovifa
Primary DI
04573277310111
Version / Model
imovifa
Company Name
CREWT MEDICAL SYSTEMS, INC.
Labeler DUNS
692045844
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-16
Public Version
1
Public Version Date
2023-06-26
Public Version Status
New
Public Device Record Key
afee792e-ab9a-48eb-a26c-c6569adeaa9e

Device Description

An imovifa is used to perform visual field testing by recording the patient's reaction to small light spots automatically displayed at various positions.

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
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
HPT Perimeter, Automatic, Ac-Powered

GMDN Terms

Code Name
16918 Perimeter, automatic

Identifiers

Type ID
Primary 04573277310111

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity