Suction swabs (also called suction tips or absorbent suction sticks) are single-use medical/clinical accessories designed to absorb fluids while allowing suction systems to remove liquids, debris, or foams from a treatment site. They combine an absorbent tip with a rigid or semi-rigid handle that connects to a suction tube or fits into a handpiece, enabling rapid fluid control in tight spaces.
Most suction swabs are composed of two primary parts: the tip (absorbent material) and the handle/core (plastic or metal adapter). Tip materials vary (foam, cotton, polyurethane, silicone), and handles can be straight, angled, or flexible to reach different anatomical or equipment positions.
Sizes are typically specified by tip diameter and overall length (for example, 4 mm × 80 mm). Connectors are made to fit standard suction tubing (e.g., Luer-compatible or universal tapered adapters). Always confirm compatibility with your suction system before purchase.
Suction swabs are widely used wherever precise fluid control is needed. Their lightweight, single-use design reduces cross-contamination risk and speeds procedures.
Selecting the correct suction swab requires matching tip material, absorbency, size, and connector to the clinical task. Below are key selection criteria with practical advice.
Type | Tip material | Absorbency | Typical uses | Sterility option |
Foam swab | Open-cell polyurethane foam | High | Surgical/dental bleeding control | Sterile & non-sterile |
Cotton swab | Cotton (compressed) | Medium | Wound blotting, oral care | Sterile & non-sterile |
Silicone-tip swab | Medical-grade silicone | Low (non-absorbent) | Delicate wiping, positioning | Usually non-sterile (sterile options exist) |
Hydrophilic coated swab | Polyurethane with hydrophilic finish | Very high | Rapid fluid uptake, heavy exudate | Sterile options |
Packaging ranges from bulk boxes of non-sterile swabs to individually sealed sterile pouches. Labels should include lot number, expiry date, sterilization method (if applicable), and intended single-use designation. For markets with regulatory oversight, manufacturers commonly follow standards such as ISO 13485 for quality systems or provide CE/FDA documentation where required by local law; buyers should request certificates and test reports as part of supplier qualification.
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