NSN	6515-01-655-9514
Manufacturer	TyTek Medical
Model	PneumoDart 14G × 3.25″, Veress safety tip.
Country of origin	USA
Product type	Medical device
Features	14G × 3.25″ (approximately 8.25 cm); Veress safety tip; Luer-lock cap for active removal of air or blood; CoTCCC-recommended dimensions; NSN 6515-01-655-9514.
Certifications	FDA cleared; ISO 13485 certified.
Sterility	Sterile
Shelf Life	3 years.
Use	Needle decompression for tension pneumothorax; management of chest trauma in emergency and tactical medical settings.
Warnings	For use by trained professionals only. Needle decompression should only be performed for tension pneumothorax in accordance with the applicable protocol.
Storage	Store in a dry place at room temperature in the original packaging.
Product Dimensions	14G x 3,25″ (apie 8,25 cm)
Color	Skaidri
Contents	5 × 5 cm; hydrogel thickness: approximately 3.5 mm.

NSN	6515-01-541-0635
Manufacturer	TyTek Medical
Model	TPAK 14G x 3,25″Decompression needle.
Country of origin	USA
Product type	Medical device
Features	14G x 3,25″ (8,25 cm); CoTCCC Recommended dimensions; needle-free flash chamber for instant confirmation;
Certifications	FDA registration (GUDID), EU Declaration of Conformity (MDR), UDI labeling.
Sterility	Sterile
Use	Needle decompression for tension pneumothorax in tactical and military medicine and emergency medical settings. Single-use..
Warnings	For use by trained professionals only. Needle decompression should be performed only in cases of tension pneumothorax and in accordance with the applicable protocol. Immediate medical attention is required following the procedure..
Storage	Store in a dry place at room temperature in the original packaging.
Product Dimensions	14G × 3,25″ (8,25 cm)
Color	Skaidri
Contents	1 × sterile TPAK® TM-303 14G × 3.25” decompression needle with catheter in a protective case..

Manufacturer	TyTek Medical
Model	XTricate Lyte Soft Emergency Stretcher
Country of origin	USA
Product type	Medical device
Features	Lightweight, compact, single-use soft emergency stretcher designed for rapid casualty transport; maximum load tested by an independent laboratory – 226 kg; made from durable polypropylene webbing and lightweight non-woven polypropylene fabric; reinforced polyester stitching; 4 large carrying handles on each side and 2 handles at both the head and foot ends, providing a total of 12 carrying handles.
Sterility	Non-sterile.
Use	Rapid casualty transfer and extraction from hazardous areas in tactical, rescue, and industrial situations.
Warnings	Inspect the condition of the fabric and carrying handles before use. Casualty transfer should only be performed by trained personnel.
Storage	Store folded in a dry place.
Contents	1 × XTricate Lyte TM-512 soft emergency stretcher.

NSN	6510-01-642-6212
Manufacturer	North American Rescue, LLC
Model	HyFin® Vent Chest Seal Twin Pack
Product type	Medical device
Country of origin	USA
Certifications	TCCC ir TECC gairės; EMS Standard of Care; JAV patent 7,504,549
Sterility	Sterile
Use	Use to seal penetrating chest wounds in accordance with the manufacturer’s instructions for use and applicable first aid and emergency medical protocols. Before applying the seal, clean the wound area with the gauze pad included in the kit. Position the transparent seal so that the venting system is correctly aligned over the wound. After application, continuously monitor the patient’s respiratory condition.
Contents	2 × HyFin® Vent Chest Seals + 1 gauze pad for cleaning the wound area with each seal.
Warnings	Use the device in accordance with the manufacturer’s instructions for use and applicable medical care protocols. After applying the seal, continuously monitor the patient for any deterioration in respiratory condition and, if necessary, take the measures specified in the applicable protocols. Do not use if the sterile packaging is damaged or if the expiry date indicated on the packaging has passed. For single use only. Do not reuse.
Storage	Laikyti originalioje nepažeistoje pakuotėje, laikantis gamintojo pakuotėje ir naudojimo instrukcijoje nurodytų laikymo reikalavimų. Konkrečios laikymo temperatūros ir santykinės drėgmės ribos viešame gamintojo produkto aprašyme nenurodytos.