FDA UDI In Commercial Distribution 🇺🇸 United States

HemoScreen

DI: 07290016991000 · Model: HemoScreen 200 · PIXCELL MEDICAL TECHNOLOGIES LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HemoScreen
Primary DI
07290016991000
Version / Model
HemoScreen 200
Company Name
PIXCELL MEDICAL TECHNOLOGIES LTD
Labeler DUNS
532623092
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-14
Public Version
3
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
bbe1d947-a863-4aac-93d2-9253218ddead

Device Description

The HemoScreen is a quantitative automated hematology analyzer intended for in vitro diagnostic point-of-care (POC) use to classify and enumerate the following parameters for capillary and venous whole blood (K2 EDTA anticoagulated) in adults and children at least 2 years of age: WBC, RBC, HGB, HCT, MCV, MCH, MCHC, RDW, PLT, MPV NEUT%, NEUT#, LYMPH%, LYMP#, MONO%, MONO#, EO%, EO#, BASO%, and BASO#. The HemoScreen analyzer is indicated for use in clinical laboratories, and in POC settings

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
GKZ Counter, Differential Cell

GMDN Terms

Code Name
35476 Haematological cell analyser IVD

Identifiers

Type ID
Primary 07290016991000

Customer Contacts

Phone
+97249593516

Premarket Submissions

Submission Number Supplement Number
K180020 000