Please click here to check who's online and chat with them.

Systester Heat Seal Testing

Supplier From China
Nov-13-17

Applies to best parameters determination of heat sealability of various kinds of film. Heat sealability of film depends on temperature, pressure and heat time and the hsl-6001 heat seal tester is widely used in food and pharmaceutical packaging industries.

Features
1: our own patent technology
2: embedded system control
3: touch screen operation, easy to operate
4: tft lcd display, ui flattening design
5: dual heat jaws, temperature controlled independently
6: micro-printer prints mini-report
7: pressure easy to adjust, heat temperature and time touch screen input.
8: emergency stop button, safety design to prevent burns
9: over temperature protection, over pressure protection
10: silence working
11: db9 rs232 communication port.
12: dsm system is optional(laboratory management information system), easy to manage and share test data.


Recent User Reviews

This user has not received any reviews yet!

Verification Status


 
 
Contact Supplier
Renew

More Items Similiar to: Systester Heat Seal Testing

Nov-01-23
Supplier From Huissen, Gelderland, Netherlands
 
Bayer Contour next teststrip

For use with Bayer's Contour XT & Contour Next glucose meter.

Composition
21% FAD-Glucose-Dehydrogenase (Aspergillus sp, 4.0 U/test strip).
54% mediator
25% non-reactive components

Do not use if package seal is damaged or missing.
Aug-05-21
Supplier From Dubai, United Arab Emirates
Sep-15-20
 
Material: - medical grade paper with technic 60gsm or 70gsm , - transparent PET/PP multi-layer copolymer film with tined-blue tinted-green or tinted-purple color. Sterilization: - Steam, - Ethylene Oxide (EO), - and Formaldehyde(FORM) indicator available upon request
Jan-12-21
Supplier From Faridabad, Haryana, India
Apr-25-13
 
Heat-sealing flat/gusseted/tyvek reel/pouch for packaging

1. Application:
Used as sterilization package for medical devices, quick and secure closing of a pack with a heat sealer, suitable for packaging extra long products or creating individual pouches of special length. The indicator imprints can indicate the process of the sterilization, judge the effect of the sterilization.

2. Materials:
Medical grade paper + see-through medical film, with incorporating steam and eo indicator imprints. (tyvek material is also available)

3. Sterilization method:
Eo or steam

4. Type:
Flat (plain) and gusseted reels for selection.

5. Standard:
In compliance with iso11607 and en868 standard, the indicator ink used is in full compliance with iso. 11140-1.

6. Advantage:
(1) can be cut into different length according to the size of the device to be sterilized, can create individual pouches of different size, very convenience.
(2) easy identification of contents through the see-through film.
(3) the indicator imprints are subjected to same sterilization conditions as the packaged product, and will undergo a distinct change in color when subjected to the sterilization process.
(4) easy to seal with all types of heat sealing machines.

7. Regular size:
A) heat-sealing flat reels
Width 50mm, 75mm, 100mm, 150mm, 200mm, 250mm, 300mm, 400mm * 200m length / roll
B) heat-sealing gusseted reels
Width 75mm, 100mm, 150mm, 200mm, 250mm, 300mm, 400mm * 100m length / roll with different wide gusset
C) tyvek reels
Width 75mm, 100mm, 150mm, 200mm, 250mm, 300mm, 400mm * 70m length/ roll
Mar-11-10
 
Canine brucella ab rapid test is a lateral flow immunoassay for quick detection of brucella canis in serum. Welcome your enquiry!

Specifications
Specimens: serum
Shelf life: 18 months
Storage temperature: room temperature(2-30c degree)

10 tests per kit, sealed in foil pouch
May-16-21
Buyer From Lahore, Pakistan
Aug-22-20

Covid-19 Igm/igg Antibody Test

$4
MOQ: Not Specified
Supplier From Dubai, Dubai, United Arab Emirates
 
Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma
or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test.

Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling.

(A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test

(B) Price $4 EXW

(c) Origin: Canada

(d) Features:
Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection.

(E) HS code:382200

(F) 20,000 units

(g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg.
25,000 kits per pallet.
Sep-01-10
 
Rapid Influenza A + B Test Card

Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.

Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea

Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.

Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.

25 tests/kit, 40 kits/carton

Verification Status