Specifications
CLASS
Specimen Collection & Transport
SUBCLASS
Swabs & Applicators
SHIPPING NOTES
Shipping Box Outer Dimensions: 19-7/8 x 15-3/4 x 9-1/2 inches. Shelf Pack Quantity per Shipper Box: 10. Shipper Boxes per Pallet: 42.
COUNTRY OF ORIGIN
United States
RAW MATERIAL ORIGINS
100% United States
APPLICATION
Specimen Collection Swab
USAGE
DIRECTIONS FOR USE, SPECIMEN COLLECTION
In case the swab is packaged with other items in a kit, follow all other provided instructions for use.
NOTE: Sterile gloves, protective clothing and eye-wear should be worn when collecting and handling microbiology specimens.
1. Open the pouch and take out the swab. Do not touch the sample end of the swab.
2. Collect the sample. During sampling, the swab end (tip) shall only come in contact with the suspected infection, so as to reduce contamination risks.
3. Process the swab according to internal laboratory procedure. Alternatively put the swab in the transport test tube. See Figure 1
4. If required, break the swab using a rapid, swift motion. If the swab does not break cleanly, a slight twisting motion may be required to complete separation.
5. Send the sample to the laboratory for immediate testing.
PRECAUTIONARY STATEMENTS
1. Carefully follow the instructions for use.
2. When using the device, pressure applied during sampling shall be light since the stick material
is breakable.
3. The fiber adhesion to the stick is tested for instantaneous sampling: a longer contact between
the swab and the sampling area might cause the fiber to come out.
4. If the swab is submitted to a chemical or physical sterilizing or micro-biostatic process, its
intended functioning could be compromised.
5. Product can not be reused or re-sterilized.
*USAGE / SAFETY STATEMENT
Test Swabs are sterile and ready-for-use systems intended for clinical samples drawing. The swab is suitable for short contact with the human body. Product should be used as directed. Refer to manufacturer's Instructions for Use (IFU) for complete and accurate information.
REGULATORY NOTICE & RESTRICTIONS
510(k) Exempt. Product Code KXG. Class 1 Medical Device. Approved Jurisdictions: United States, Canada, and European Union. Specimens collected for clinical investigations should be collected and handled following published anuals and guidelines. Specific requirements for the shipment and handling of specimens should be in full compliance with state and federal regulations. Shipping of specimens within medical institutions should comply with internal guidelines of the institution.
DISCLAIMER
LIMITATIONS
1. In the laboratory, wear protective gloves and other protection commensurate with universal precautions when handling clinical specimens. Observe Biosafety recommendations when handling or analyzing patient samples.
2. Condition, timing, and volume of specimen collected for clinical investigation are significant variables in obtaining reliable results. Follow recommended guidelines for specimen collection.
3. Test Swabs must be used by skilled personnel only.
NOTE: Do not use excessive force, pressure or bending when collecting swab samples from patients as this may result in accidental breakage of the swab shaft. Swab shafts often exhibit diameter changes to facilitate different sampling requirements. Swab shafts may also have a molded breakpoint point designed for intentional breakage of the swab into a transport tube. Use a swift, deliberate motion when intentionally breaking the swab at the break off portion for insertion
WARNINGS
1. This product is for single use only; reuse may cause a risk of infection and/or inaccurate results.
2. Do not re-sterilize unused swabs.
3. Do not re-pack.
4. Not suitable for any other application than intended use.
5. The use of this product in association with a rapid diagnostic kit or with diagnostic instrumentation should be previously validated by the user.
6. Do not use if the swab is visibly damaged (i.e., if the swab tip or swab shaft is broken).
7. Do not use excessive force, pressure or bending when collecting swab samples from patients as this may result in accidental breakage of the swab shaft.
8. Directions for use must be followed carefully. The manufacturer cannot be held responsible for any unauthorized or unqualified use of the product.
9. To be handled by trained personnel only.
10. It must be assumed that all specimens contain infectious micro-organisms; therefore all specimens must be handled with appropriate precautions. After use, tubes and swabs must be disposed of according to laboratory regulations for infectious waste.
Refer to manufacturer's Instructions for Use (IFU) above for complete and accurate information.
MATERIAL
Polyamide (Nylon) Flocked Tip, Polypropylene Handle
DIAMETER
4.06 mm (Max Tip Diameter) / 2.4 mm (Handle Diameter)
LENGTH
152 mm (Overall Length) / 18.42 mm (Tip Length) /
QUALITY CERTIFICATION / COMPLIANCE
ISO 13485, FDA Registered
APPEARANCE
The shaft and tip appear white. A slight yellowing of the tip is a well-known phenomenon. This could be due to many factors: to the type of raw material, to the product sterilization treatment, to the product natural aging. Therefore product yellowing is not necessarily indicative of product deterioration.
WASTE DISPOSAL
Unused swabs may be considered as non hazardous waste and disposed of accordingly. Dispose of used swabs as well as any other contaminated disposable materials following procedures for infectious or potentially infectious products. It is the responsibility of each laboratory to handle waste and effluents produced according to their nature and degree of hazardousness and to treat and dispose of them (or have them treated and disposed of) in accordance with applicable regulations.
STERILIZATION METHOD
Ethylene Oxide Gas
FLOCK MATERIAL
Polyamide (Nylon)