FDA UDI In Commercial Distribution 🇺🇸 United States

DYSIS Ultra

DI: 05060477110065 · Model: DYS402 - DYSIS Ultra · DYSIS MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DYSIS Ultra
Primary DI
05060477110065
Version / Model
DYS402 - DYSIS Ultra
Company Name
DYSIS MEDICAL LIMITED
Labeler DUNS
424589138
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-25
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
8418f2dc-f04f-40d3-b655-e461800b47f6

Device Description

DYSIS with Pseudo-Colour Imaging (PCI) is a digital colposcope designed to image the cervix and lower genital tract under illumination and magnification. Colposcopy is indicated for women with an abnormal Pap smear in order to affirm normality or detect abnormal appearances consistent with neoplasia, often with directed biopsy. The PCI feature is an adjunctive tool for displaying areas of acetowhitening. It is a tool that should NOT be used as a substitute for a thorough colposcopic evaluation. The system consists of 7 components; PC, BASE Assembly, Optical ARM Assembly (ARMO), Display ARM Assembly (ARMD), Optical Head Unit, Clinician Touch Screen Monitor and Patients Monitor.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HEX Colposcope (And Colpomicroscope)

GMDN Terms

Code Name
10960 Colposcope

Identifiers

Type ID
Package 15060477110062
Primary 05060477110065

Premarket Submissions

Submission Number Supplement Number
K092433 000