5-Part Hematology Analyzer hmanga siam a ni

5-Part Hematology Analyzer hmanga siam a ni

5-Part Hematology Analyzer Calibrator hi stable, multi-parameter reference material a ni a, biological cellular components humhalh hmanga siam a ni a, automated differential cell counter te tehna dik leh dik loh a align leh verify turin a siam a ni. Thisen zat kimchang leh thisen var cell differential parameter hrang hrangah target value assignment rintlak tak a pe a, international standard reference methods-a direct metrological traceability a tichiang a ni.

Product Thuhmahruai .

5-Part Hematology Analyzer Calibrator hi stable, multi-parameter reference material a ni a, biological cellular components humhalh hmanga siam a ni a, automated differential cell counter te tehna dik leh dik loh a align leh verify turin a siam a ni. Thisen zat kimchang leh thisen var cell differential parameter hrang hrangah target value assignment rintlak tak a pe a, international standard reference methods-a direct metrological traceability a tichiang a ni.

 

Hematology Control / Calibrator te hi eng nge ni?

 

Clinical laboratory diagnostics-ah chuan calibrator leh control te hian reference function hrang hrang an thawk a:

Calibrators te pawh a awminstrument sensor signal leh physical cell concentration tak tak inkara mathematical relationship sawifiah a, primary measurement baseline din.

Controls tenitin routine analytical precision leh system stability chu hun rei tak chhung enfiah a, system gain settings siam danglam lovin measurement te chu set standard deviation limits chhungah a awm reng em tih enfiah thin.

 

Hematology Quality Control-a a chanvo

 

Calibration dik tak hian thisen cell chhiar nawn leh theih nan baseline mamawh a pe a:

System Recalibration tih dan tur: 1.1.Re- chuan fluidic maintenance lian tham, optical realignment, emaw component thlak danglam hnuah analytical accuracy a din thin.

Reagent Lot inthlak danglamna: 1.1.Diluent, lyse, emaw cleaning solutions production lots inthlak danglamnaah baseline shift awm thei te chu a siamthat thin.

Metroological Traceability hmanga zawn chhuah theihna:Nitin routine laboratory measurement te chu ISO 17511 guidelines hnuaia standardized primary reference methods te nen direct in a thlunzawm thin.

Shift siamthat dan tur:Nitin statistical quality control monitoring neih chhunga systematic calibration drift hmuhchhuah te chu a chinfel sak thin.

 

Control Level / A hman dan tur

 

Calibrator-te chuan central analytical accuracy an set laiin, companion quality control-te chuan operational range hrang hranga performance an verify thung:
Level hniam tak a ni
Detector sensitivity leh low-end linearity a enkawl a, hei hi leukopenia na tak, thrombocytopenia, emaw anemia na tak nei clinical sample endikna atana pawimawh tak a ni.
Normal Level a ni
Reference population hrisel tak takte tan standard physiological range chhunga routine analytical precision a verify a, nitin operational benchmark atan a thawk.
Level sang tak a ni
Cell concentration sang takah system linearity leh optical performance a evaluate a, leukocytosis na tak emaw thrombocytosis condition na tak karah tehna dik tak a enfiah thin.

 

Control leh Calibrator te a ni

 

Mihring ziarang

Calibrator a ni

Thunun

Tum bulpui ber

Instrument calculation factors leh detector sensitivity te a siamrem thin

Measurement kalpui mek precision leh operational consistency a enfiah thin

A hman dan Frequency

Periodic (install, enkawl, lot thlak, drift) te a awm thin.

Nitin emaw, operational testing run khatah emaw

Value Assignment tih hi a ni

Standard reference method hmanga target value pekte chu tihfel a ni

Target range tihfel tawh, deviation limit pawm theih nei

System Action hmanga hmalakna

Internal gain factor leh calibration coefficient te a update thin

Instrument readiness a nemnghet emaw, operational errors a flag emaw a ni

 

Hematology Analyzers hmantlak tak tak te

 

Optical scatter, electrical impedance, leh colorimetric measurement technology hrang hranga open leh closed sampling channel atana siam:

  • Semiconductor laser scatter leh flow cytometry hmanga differential analyzer siam a ni
  • Hydrodynamic focusing hmanga impedance cell chhiar dan
  • Cyanide-free hemoglobin colorimetric tehna module hmanga siam a ni

 

Value / Parameter pek chhuah te

 

Parameter a ni

A tawi zawngin

Target Value pek dan pangngai

Hlawm khat

Thisen sen (Red Blood Cell) awm zat

RBC a ni

4.50 ± 0.15

10¹²/L

Hemoglobin awm zat

HGB

135 ± 3

g/L

Hematocrit a ni

HCT a ni

40.0 ± 1.5

%

Corpuscular Volume tih awmzia chu a ni

MCV a ni

88.0 ± 2.0

fL

Thisen var Cell chhiar zat

WBC a ni

7.50 ± 0.30

10⁹/L

Neutrophil za zela 100 vel

NEUT% a ni.

60.0 ± 3.0

%

Lymphocyte Za zela 100

LYMPH% a ni.

28.0 ± 2.5

%

Monocyte za zela 100

MONO% 100% a ni.

6.0 ± 1.5

%

Eosinophil Za zela 100

EO% a ni.

4.0 ± 1.0

%

Basophil Za zela 100

BASO% 100% a ni.

2.0 ± 0.8

%

Platelet awm zat

PLT

240 ± 15

10⁹/L

 

Product chungchang chi hrang hrang

 

Nihphung

Technical lam hawi zawng zawng

Taksa dinhmun

Suspended fluid hman theihna tura inpeih-

Matrix Component hmanga siam a ni

Biological cell suspensions vawn that a ni

Volume chu fill rawh

Vial khatah 3.0 mL a ni

Traceability Standard a ni

ISO 17511 zawm tur reference methods te

Packaging Configuration hrang hrang te

2 x 3.0 mL / 4 x 3.0 mL / OEM bulk package siam chhuah a ni

 

Storage & Stability a ni

 

A dahna Temperature: 1.1.2℃leh 8℃inkar ah dinglam hawiin dah rawh . Freezing leh direct light exposure atanga venhim.
A hawn loh Shelf Life:A siam chhuah atanga ni 105 chhungin 2℃atanga 8℃thlenga dah chhunzawm zel a nih chuan .
Open-Vial a nghet thei ang bera awm:Ni 7 chhung chu strict aseptic handling hnuaiah leh sample lak hnuah 2℃atanga 8℃storage-ah kir leh nghal tur a ni.
Thermal Logistics hmanga thil tih dan tur:Temperature-monitored cold-chain container 2℃leh 8℃inkar enkawl hmanga thawn chhuah a ni.

 

Quality Assurance neih a ni

 

Reference Method Alignment neih dan tur: 1.1.Standardized microscopic reference method leh verified master reference instrument hmanga value pek te.
Homogeneity Control-na chu: 1.1.Lot tin hian tihchhuah hmain vial-to-vial consistency testing leh coefficient of variation verification an nei vek a ni.
Thil siam chhuah dan zawm dan:Diagnostic medical devices atana ISO 13485 quality management system hnuaia siam a ni.
Biological Safety chungchang: 1.1.Source materials te chu HBsAg, anti-HCV, leh anti-HIV antibodies te tan non-reactive test a ni.

 

FAQ

 

Q: Engtikah nge calibration hi tih tur?

A: Instrument dah hmasak ber, optical emaw fluidic maintenance lian tak neih zawhah, systematic drift lantir thei reagent lot switch-naah emaw, nitin quality control result chu defined control range pawna a tlak fo chuan calibration a ngai a ni.

Q: Calibrator hi open leh closed vial aspiration pahnih nen a inmil em?

A: Ni e, fluid suspension hi manual open-vial mode leh automated closed-vial sampling system-ah te pawh viscosity leh cellular distribution inang tlang taka vawng reng turin siam a ni.

Q: Parameter tin tan engtin nge target value siam a nih?

A: Assigned value te hi ISO 17511 metrological traceability guidelines angin siam a ni a, designated reference measurement procedure leh standardized master analyzer hmangin siam a ni.

Q: Sample lak hmain eng inbuatsaihna nge mamawh?

A: Vial chu kut hmangin zawi zawiin vawi tam tak invert la, uniform suspension a awm theih nan. Foam siam chhuah emaw, optical scatter reading tibuai thei micro-bubble entrapment emaw ven nan mechanical shaking rang tak pumpelh rawh.

Q: International shipping neih chhung hian engtin nge product integrity hi vawn reng a nih?

A: Shipment-ah hian insulated container, cold pack leh internal temperature monitor hmanga thuam a ni a, hei hian transit chhung zawngin 2℃atanga 8℃vel a awm reng thei a ni.

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