SAM Pelvic Sling II (Military Version)
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SAM Occlusive Chest Seal (Non-Valved)
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SAM Valved Chest Seal
Chest seal with a rigid, raised TRUFLOW valve designed for one-way evacuation of air from the chest cavity.
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- Fast delivery throughout Lithuania and Europe
- Goods are stored and shipped from Lithuania
- Special Purchasing Terms for Businesses and Organizations
- Professional assistance from product selection to configuration
| NSN | 6510-01-658-7745 |
|---|---|
| Manufacturer | SAM Medical Products |
| Model | SAM Chest Seal Valved with TRUFLOW Valve. |
| Country of origin | USA, USA |
| Product type | Medical device, Medical device |
| Features | Rigid, raised TRUFLOW valve; one-way airflow; hydrogel adhesive; oval shape; two application tabs. |
| Certificates | ISO 13485; CE; NSN 6510-01-658-7745. |
| Sterility | Sterile |
| Expiration date | 6 years. |
| Usage | Penetrating chest wounds requiring a reliable one-way air evacuation pathway. |
| Product dimensions | Tvarstis: 17,8 × 22,9 cm (7 × 9″). Pakuotė: 25,4 × 16 cm (10 × 6,3″) |
| Warnings | After applying the chest seal, monitor the casualty for signs of tension pneumothorax. Ensure that the valve is not compressed or obstructed by blood clots. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Equipment / Configuration | 1 × SAM® Chest Seal Valved 2.0 vented chest seal. |
Description
The vented chest seal is designed to reliably cover open chest wounds and help reduce the risk of tension pneumothorax. It features a rigid, raised-dome TRUFLOW valve designed to help maintain an air escape pathway even when the dressing is compressed by the patient’s clothing, stretcher, or body weight.
The one-way valve allows air to escape from the chest cavity while helping prevent air from re-entering through the wound.
The chest seal uses a hydrogel adhesive designed to provide reliable adhesion to the skin in challenging conditions, including wet or contaminated surfaces.
Its construction is intended for emergency care, tactical medicine, and prehospital environments where rapid access to a chest wound and reliable sealing are essential.
Why is the valve rigid and raised?
So it cannot be crushed shut by clothing or body weight.
Does the patient still need monitoring?
Yes – tension pneumothorax remains possible with a vented seal.
Technical Specifications
| NSN | 6510-01-658-7745 |
|---|---|
| Manufacturer | SAM Medical Products |
| Model | SAM Chest Seal Valved with TRUFLOW Valve. |
| Country of origin | USA, USA |
| Product type | Medical device, Medical device |
| Features | Rigid, raised TRUFLOW valve; one-way airflow; hydrogel adhesive; oval shape; two application tabs. |
| Certificates | ISO 13485; CE; NSN 6510-01-658-7745. |
| Sterility | Sterile |
| Expiration date | 6 years. |
| Usage | Penetrating chest wounds requiring a reliable one-way air evacuation pathway. |
| Product dimensions | Tvarstis: 17,8 × 22,9 cm (7 × 9″). Pakuotė: 25,4 × 16 cm (10 × 6,3″) |
| Warnings | After applying the chest seal, monitor the casualty for signs of tension pneumothorax. Ensure that the valve is not compressed or obstructed by blood clots. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Equipment / Configuration | 1 × SAM® Chest Seal Valved 2.0 vented chest seal. |
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HEMGUARD 4″ Targeted Pressure Bandage
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| NSN | 6515-01-732-6982 |
|---|---|
| Manufacturer | 6:8 Medical Solutions LLC |
| Model | HEMGUARD 4″ Targeted Pressure Bandage |
| Country of origin | USA, USA |
| Product type | Medical device, Medical device |
| Features | Targeted pressure applicator; four-way strap routing; bidirectional mechanical advantage; weight approximately 113 g (4 oz); FDA listed and CE marked. |
| Certificates | U.S.-patented design. |
| Sterility | Sterile |
| Expiration date | 5 years |
| Usage | Neck, axillary, and groin wounds; amputations; maintaining pressure on packed wounds during evacuation. Single-use. |
| Warnings | The dressing does not replace a tourniquet in cases of life-threatening extremity bleeding. The wound must be properly packed before applying the dressing. |
| Storage | Store in a dry place in the original packaging. |
| Product dimensions | 10 cm (4″) × 163 cm (64″) |
| Color | Juoda |
| Equipment / Configuration | 1 × sterile HEMGUARD® 4″ pressure dressing in an individual vacuum-sealed package. |
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NIO Adult Intraosseous Access Device (12 years and over)
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| NSN | 6515-01-667-2884 |
|---|---|
| Manufacturer | PerSys Medical (Safeguard Medical) |
| Model | NIO Adult, 15G x 25 mm |
| Country of origin | USA, USA |
| Product type | Medical device, Medical device |
| Features | 15G, 25 mm needle; automatic deployment; access in less than 10 seconds; no exposed needle; protection against accidental activation; 5-year shelf life. |
| Certificates | FDA 510(k) K142086, ISO 13485 |
| Sterility | Sterile |
| Expiration date | 5 years |
| Usage | Emergency vascular access for adults and children aged 12 years and older when intravenous access cannot be established or is not feasible. Single-use. |
| Warnings | For use by trained healthcare professionals only. Do not use in a fractured or infected bone, or in a limb where intraosseous access has already been attempted. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Product dimensions | 13,9 × 5,7 × 2,7 cm |
| Color | Mėlyna |
| Equipment / Configuration | 1 × sterile NIO Adult™ device, 1 × NIO Fixation™ securement dressing, instructions for use. |
NIO Infant Intraosseous Access Device
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| Manufacturer | PerSys Medical (Safeguard Medical) |
|---|---|
| Model | NIO Infant, stepped needle 14G–18G |
| Country of origin | USA, USA |
| Product type | Medical device, Medical device |
| Features | Stepped 14G–18G needle; tactile feedback indicating position within the bone marrow cavity; self-contained device; no exposed needle. |
| Certificates | FDA 510(k) (K190538), ISO 13485 |
| Sterility | Sterile |
| Expiration date | 5 years. |
| Usage | Emergency vascular access in infants when intravenous access cannot be established or is not feasible. |
| Warnings | Intended for use by trained healthcare professionals only. Do not use on fractured or infected bone. |
| Storage | Store in a dry place at room temperature in the original packaging. |
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SAM ThoraSite chest cavity needle decompression system
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| NSN | 6515-01-655-9514 |
|---|---|
| Manufacturer | SAM Medical Products |
| Model | SAM ThoraSite, 1-pack |
| Country of origin | USA |
| Product type | Medical Device |
| Features | Anatomical landmarking template; helps identify the correct intercostal space; supplied individually (1 unit). |
| Certificates | FDA |
| Sterile | Anatomical landmarking template; helps identify the correct intercostal space; supplied individually (1 unit). |
| Expiration date | 5 years |
| Usage | Identification of needle decompression and lateral thoracostomy sites in emergency, tactical, and military medical settings. |
| Warnings | The device is intended for use by trained professionals and does not replace clinical assessment. Needle decompression should only be performed in accordance with current protocols. |
| Storage | Store in a dry place in the original packaging. |
| Equipment / Configuration | 1pcs. |
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Stream Defence Thermal Container M29DCe
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| NSN | 4110-99-362-8335 |
|---|---|
| Manufacturer | Stream Defence |
| Model | M29DCe |
| Country of origin | United Kingdom, United Kingdom |
| Product type | Thermal container, Thermal container |
| Features | Active cooling temperature-controlled container designed for transporting blood components, medicines, and other temperature-sensitive medical cargo. Maintains a stable temperature, features an integrated battery and data logging functionality, and operates from both AC and DC power sources. Its durable housing is designed to meet the requirements of emergency medical services, military medical units, and field hospitals. |
| Certificates | EMC Directive 2014/30/EU, Low Voltage Directive 2014/35/EU |
| Sterility | Non-sterile |
| Usage | Reusable. For the transport and storage of blood products, vaccines, and temperature-sensitive medicines in field and transport conditions. |
| Warnings | When transporting blood products and medicines, the temperature must be continuously monitored, and the manufacturer’s instructions and healthcare facility protocols must be followed. |
| Storage | Store in a dry place; check the unit’s operation and power supply before use. |
| Product dimensions | 816 × 540 × 320 mm |
| Color | Juoda |
| Equipment / Configuration | 1 × M29DCe temperature-controlled container, 100–240 V AC power supply, SD card, Stream VISI software, internal bag, user manual. |
