Curaplex

Basic Information

• Brand Name: Curaplex
• Primary DI: 00812277037401
• Version / Model: 14781
• Catalog Number: 14781
• Company Name: BOUND TREE MEDICAL, LLC
• Labeler DUNS: 070556204
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2022-12-30
• Public Version: 1
• Public Version Date: 2023-01-09
• Public Version Status: New
• Public Device Record Key: 096bac68-8cf2-4efa-a90b-2b18892a359e

Device Description

Curaplex Folding Scoop Stretcher, w/Straps (Load Limit 350lb)

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: Yes
• PM Exempt: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
FPP	STRETCHER, HAND-CARRIED	General Hospital	880.6900	1

GMDN Terms

Code	Name	Definition	Implantable	Status
13673	Spine board	A flat, stiff device intended to be placed under a patient (the patient is usually strapped to this device) to ensure spinal immobilization when a spinal injury is suspected. This device is often used in combination with a head/neck immobilizing device that is also typically fixed or strapped to it. It is typically used after serious accidents and for transport of the patient on a stretcher. It is typically made of x-ray translucent/non-ferromagnetically active materials that allow x-ray and magnetic resonance imaging (MRI) and comes in various sizes. This is a reusable device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	00812277038668	GS1	CS	1	In Commercial Distribution
Primary	00812277037401	GS1