Radiolucent Paediatric Spinal Extrication and Immobilisation
The Extrication Device Paediatric EM0110 (VM-KEDP) is a Kendrick-type extrication device designed for immobilisation and safe extrication of paediatric patients from vehicles when spinal injury is suspected, or when rib, hip, or pelvic fractures are present. Vehicle extrication of a patient with a suspected spinal injury requires the spine to be held in neutral alignment throughout the movement from seated position to horizontal on a stretcher — an operation that cannot be safely achieved with a cervical collar alone. The KED device wraps around the patient’s torso and head, securing the thoracic and lumbar spine, pelvis, and head as a single rigid unit before movement begins. The EM0110 is specifically sized for paediatric patients, addressing the anatomical differences between children and adults that make adult extrication devices inappropriate for paediatric use. The device is constructed from strengthened Oxford cloth with bamboo reinforcement — a material combination that is radiolucent, enabling X-ray imaging of the thorax, spine, or pelvis without device removal upon arrival at hospital.
Colour-Coded Straps, Fold-Back Chest Access, and Pelvic Splint Configuration
The EM0110’s sewn-in securing straps are colour-coded for rapid sequencing during application under stress, with snap-lock buckles that engage quickly and securely without fumbling. The adjustable, fold-back chest flap panels allow access to the patient’s chest for cardiac monitoring electrode placement or defibrillation pad positioning without removing or repositioning the device — a clinically significant feature in paediatric trauma where concurrent cardiac assessment may be required. Two head straps secure the patient’s head to the device, maintaining cervical spine alignment during extrication and transport. By simple inversion of the device, the EM0110 can be configured as a hip and pelvic splint — extending its clinical utility beyond vehicle extrication to ground-level and confined-space entrapment scenarios. The device can also be adapted for use on small children and pregnant women, providing a versatile paediatric and special-patient extrication solution within a single unit.
Construction, Accessories, and Clinical Deployment
The EM0110 is manufactured from strengthened Oxford cloth reinforced with bamboo slats, nylon webbing, and snap-lock buckles — materials selected for durability, flexibility under clinical handling, and radiolucency. Integrated carrying handles allow the device and secured patient to be gripped and moved safely during extrication. Each unit is supplied with a carry bag, user instruction manual, 2×head straps, and a positioning pad. Product dimensions are 61×64×3cm open and 61×22×10cm folded, with a net weight of 2kg. Manufactured to ISO 13485 quality management standards and certified CE to (EU) 2017/745 Medical Device Regulation. Functional inspection required prior to each use; annual preventative maintenance by authorised service agent. 1-year carry-in warranty. Available in South Africa from Vital Medical, the VM-KEDP is suited to emergency medical services, rescue services, paediatric trauma teams, and any clinical deployment where paediatric vehicle extrication or spinal immobilisation is required.
TECHNICAL SPECIFICATIONS TABLE
| Specification | Detail |
|---|---|
| Manufacturer Reference | EM0110 |
| SKU | VM-KEDP |
| Type | Paediatric extrication device (KED) |
| Material | Strengthened Oxford cloth, bamboo reinforcement, nylon webbing, snap-lock buckles |
| Radiolucent | Yes |
| Securing Straps | Sewn-in, colour-coded with snap-lock buckles |
| Head Straps | 2 (included) |
| Chest Access | Adjustable fold-back sides |
| Hip/Pelvic Splint | Yes — by simple inversion |
| Carrying Handles | Integrated |
| Product Dimensions | 61×64×3cm |
| Folded Dimensions | 61×22×10cm |
| Packing Dimensions | 65×25×10cm |
| Net Weight | 2kg |
| Gross Weight | 2.5kg |
| Included Accessories | Carry bag, user instruction manual, 2×head straps, 1×positioning pad |
| Quality System | ISO 13485 |
| Certification | CE — (EU) 2017/745 MDR |
| Maintenance Interval | Annual — authorised service agent |
| Warranty | 1 year carry-in |

