Microbiology MID UN3373 Safety Data Sheet (SDS)

Catalogue Number Product Name
12210102 Molecular Alphavirus and Flavivirus
12220102 Molecular Bordetella pertussis
12230102 Molecular C. trachomatis and N. gonorrhoeae
12430102 Molecular Coronavirus SARS-CoV-2
12240102 Molecular Cytomegalovirus
12250102 Molecular Enterovirus
12260102 Molecular Gastrointestinal Pathogens – Bacteria
12270102 Molecular Gastrointestinal Pathogens – Parasites
12280102 Molecular Gastrointestinal Pathogens – Viral
12290102 Molecular Hepatitis B Virus DNA
12300102 Molecular Hepatitis C Virus RNA
12310102 Molecular Hepatitis C Virus RNA Genotyping
12320102 Molecular Herpes simplex virus type 1 and 2
12330102 Molecular HIV-1 RNA
12340102 Molecular Human Papillomavirus DNA
12350102 Molecular Influenza
12360102 Molecular M. tuberculosis / M. avium complex
12470102 Molecular Malaria
12370102 Molecular mec A/nuc gene
12380102 Molecular Neisseria meningitidis
12390102 Molecular Rapid Diagnostics Influenza/RSV
12400102 Molecular Respiratory Pathogens
12480102 Molecular Sexually Transmitted Pathogens
12410102 Molecular Vaccine Preventable Pathogens
12420102
Molecular Varicella zoster virus

Recommended use: Quality Assurance/Proficiency Testing programs. Not to be used in the treatment or diagnosis of patients.

Hazard Identification

Chemical hazard: Not applicable

Environmental hazard: Not applicable

Health hazard: Biological Substance, Category B

These samples must be considered as potentially biohazard and should be handled appropriately and with care.   The participant is responsible for the safe handling, storage and disposal of RCPAQAP proficiency testing materials in such a way that ensures that the proficiency testing materials will not cause any harm to any person.

The participant understands and acknowledges that, given the nature and characteristics of RCPAQAP proficiency testing materials;

  • laboratory staff should be trained in the handling of infectious materials.
  • proficiency testing materials should be processed in a laboratory environment as identified by the relevant legislative requirements.
  • they are aware of all matters that concern the safe handling, storage and disposal of proficiency testing materials.
  • they have the facilities and processes required for the safe handling, storage and disposal of proficiency testing materials.
  • that they follow Standard Safety Precautions when handling potentially infectious materials.
  • they utilise Personal Protective Equipment (PPE) as identified by the relevant legislative requirements for the routine handling of potentially infectious materials.

Composition and Information on Ingredients

Products contain the below components:

CAS# Component Percentage Exposure Limit
Not Applicable Microbial cultures 0-100% None established
Not Applicable Human fluids and tissue 0-100% None established
Not Applicable Transport medium 0-100% None established

First-aid Measures

If accidental contact with material occurs, laboratory staff should follow appropriate first aid procedures for exposure to an equivalent clinical specimen. Following exposure, medical advice should be sought. If accidental spillage occurs, follow routine procedures for clean-up of potentially biohazardous materials.

Firefighting Measures

Not applicable, not flammable.

Accidental Release Measures

Personal protective equipment such as gloves, a gown and protective eyewear should be used before cleaning any spills. Dispose of any sharps in a safe disposal system. Clean the area with absorbent paper and clean excess with suitable disinfectant (such as bleach or 70% alcohol).

Handling and Storage

On arrival, samples should be stored as per instructions provided. Samples have been shown to be stable at the nominated transport temperature.

Samples should be re-constituted or prepared according to the Survey Instructions provided.

Exposure Controls and Personal Protection

Samples are generally intended for processing in a clinical laboratory facility and should be handled in the same manner as routine patient samples using universal precautions and appropriate personal protective equipment. Biosafety Level 2 precautions at a minimum should be used in laboratory settings. In point of care (non-laboratory) settings Biosafety Level 1 precautions at a minimum should be used.

Physical and Chemical Properties

Cervical cells in PreservCyt solution – Clear to slightly opaque liquid, colourless, mild odour

Human serum/plasma: straw colour and odourless, pH neutral

Human whole blood: red colour and slightly metallic odour, pH neutral

Inactivated culture materials – clear to pink and odourless, pH neutral

Lyophilised serum/urine/CSF/respiratory/broth – white/straw colour powder, pH neutral

Lyophilised stimulated stool – brown/black colour powder, pH neutral

Simulated stool: light to dark brown solution and mild to odourless

Stability and Reactivity

This material is stable under normal temperatures and pressures, is non-corrosive, and polymerization will not occur.

Conditions to avoid: Avoid excess heat.

Toxicological Information

These samples are potentially infectious and may be positive for hepatitis B, hepatitis C virus, human immunodeficiency virus (anti-HIV-1/HIV-2) or other infectious diseases.

Ecological Information

Same biodegradability as human blood, urine and other bodily fluids.

Disposal Information

Dispose as clinical waste in suitably identified containers using a registered clinical waste disposal contractor (same as for patient samples).

Transport Information

Proper Shipping Name: Biological Substance, Category B

UN Number: UN3373

Hazard Class/Packing Group: Category B

Labels Required: UN3373

IATA Packaging Requirements: IATA compliant to PI 650 requirements.

Regulatory Information

Not Applicable.

Other Information

Reviewed annually as part of the RCPAQAP compliance with ISO/IEC 17043

The information provided in this document is believed to be accurate and represents the best information currently available to us. The RCPAQAP make no warranty or merchantability or any other warranty, express or implied, with respect to such information, and we assume no liability from its use. Users should make their own investigations to determine the suitability of the information for their particular purpose. In no event shall the RCPAQAP be liable for any claims, losses or damages of any third party or for lost profits or any special, indirect, incidental, consequential or exemplary damages, arising from the use of this product or the information contained in this Material Safety Data Sheet.