CE Diagnostic Kit for Carcinoembryonic Cea Test Kit Cea Antigen Rapid Test Carcinoembryonic AG Rapid Test Kit (whole blood)

• Customization: Available
• Type: IVD Reagent
• Certificate: CE, ISO
• Model NO.: EC-CEA
• Method: Colloidal Gold Rapid Test
• Warranty: 3 Years
• Material: Medical Grade ABS Plastic
• Package: Bottle + Carton
• Function: Early Detection
• Display: Screening
• Format: Strip+Bottle
• Name: Cea Test Kit
• Equipment: by Eye or Machine
• Reaction Time: 5-10 Seconds
• Accuracy: 99.7%
• Delivery Time: 3-5 Days
• Temperature: 4-30 Degree
• Storage: Room Temperature
• Transport Package: Carton
• Specification: 64*50*44 cm
• Trademark: evancare or OEM
• Origin: China
• HS Code: 3002150090
• Production Capacity: 100000PCS/Day

Product Description

 

Product Description

EVANCARE Diagnostic CEA Rapid Test Kits
For professional and in vitro diagnostic use only.

[INTENDED USE]

The CEA Rapid Test Cassette/Strip is a lateral flow immunoassay for the

qualitative detection of Carcinoembryonic Antigen (CEA) in human whole

blood, serum or plasma. This device is intended as an aid in monitoring

patients for disease progress or response to therapy or for the detection of

recurrent or residual disease.

[SUMMARY]

Carcinoembryonic Antigen (CEA) is a cell surface glycoprotein of

approximately 20,000 molecular weight. CEA is a blood-born protein that

was firstly noted as a specific antigen for adenocarcinoma of the colon.

Further investigations showed that CEA can be present in a variety of

cancers other than colonic, including pancreatic, gastric, lung, and breast

etc. Small amounts have also been demonstrated in secretions from the

colonic mucosa. Additionally, CEA-like substances have been reported in

normal bile from non-icteric patients. The normal CEA concentration in

human blood is <2.5 ng/mL in an adult non-smoker and <5.0 ng/mL in a

smoker. CEA Rapid tests can have significant value in the monitoring of

patients. Progressive elevations of CEA may herald tumor recurrence 3-36

months before clinical evidence of metastases. Persistent elevation in

circulating CEA following treatment is strongly indicative of occult metastatic

and/or residual disease. A persistent rising CEA value may be associated

with progressive malignant disease and poor therapeutic response. A

declining CEA value is generally indicative of a favorable prognosis and

good response to treatment. Measurement of CEA has been shown to be

clinically relevant in the follow-up management of patients with colorectal,

breast, lung, prostatic, pancreatic, ovarian, and other carcinomas. Follow-up

studies of patients with colorectal, breast and lung carcinomas suggest that

the preoperative CEA level has prognostic significance. CEA testing is not

recommended as a screening procedure to detect cancer in the general

population; however, use of the CEA test as an adjunctive test in the

prognosis and management of cancer patients is widely accepted.

 

 

 

Detailed Photos

  

Positive: *Two lines appear. One colored line should be in the control

region (C), and another apparent colored line adjacent should be in the test

region (T).

Negative: One colored line appears in the control region (C). No line

appears in the test region (T).

Invalid: Control line fails to appear. Insufficient specimen volume or

incorrect procedural techniques are the most likely reasons for control line

failure. Review the procedure and repeat the test using a new test cassette.

If the problem persists, discontinue using the lot immediately and contact

your local distributor.

 

Item No.	EVANCARE Diagnostic CEA Rapid Test Kits
Contents	Each bag:1 test cassette and 1 desiccant(cassette)                  25 cassettes+1 Buffer  /box antigen test      We can put instruction as your requirement
Format / Size	Cassette:2.5mm 3.0mm 4.0mm
Methodology	Sandwich Colloidal Gold
Assay Type	Qualitative Detection
Specimen	Antibody  (S/P/W),
Indicator	CEA Test Cassette
Storage Temperature	4-30 degree centigrade

Expiry date	3  years
Certificate	CE,ISO,FREE SALE,FDA...
Detection Limits	Home or Professional Use
Accuracy	> 99.99%
Reaction Time	3-5 min
Delivery	5-7 days
OEM Service	Available
Shipping Method	by air  or sea or international express

Company Profile

 

Certifications

 

Product Procedure

 

 

Activity Exhibition

FAQ