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Factory Sterilized Package Gather Biotech Surgical Instrument Carbon Fiber External Fixator

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Product Description

Basic Information

Model NO.1015b-a
ConditionNew
UsageFracture Fixation
Using SiteWaist
TypeExternal Fixator
ApplicationOrthopedic
GroupAdult
MaterialAlumium
Transport PackageSterilized, PE Bag, Carton Package
Specification3.0/4.0/5.0mm
Production Capacity1000pieces/Week

Product Description

Surgical Instrument External Fixator

Due to its versatility, the Hoffmann II System is indicated for complete and temporary fracture fixation for Tibia, Femur, Pelvis, and Humerus fractures. It is particularly suited for the following indications:

  • Open Fractures or Severe Soft-Tissue Injuries
  • Peri-Articular Fractures
  • Intra-Articular Fractures where a joint bridging frame can be used
  • Temporary Fracture Stabilization leading to definitive treatment
  • Poly-Trauma Patients
  • Other indications including Osteotomies and Arthrodesis
NameOrthopedic External Fixator Rod rod climp Upper & Lower Limbs Instruments
MaterialS.S
Valid Time3 Years
Licence numberCE/ISO9001
UsageMedical Fixation Equipment

Detailed Photos

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Manufacturing & Facilities

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Production Equipment

Certifications & Team

Certifications
Professional Team

Packaging & Shipping

Packaging Process

Frequently Asked Questions

FAQ Visual 1
FAQ Visual 2
What are the primary clinical indications for this external fixator?
It is primarily used for complex fracture fixation in the Tibia, Femur, Pelvis, and Humerus, especially in cases of open fractures or severe soft-tissue injuries.
What materials are used in the construction of the fixator?
The system utilizes high-grade Aluminum and Stainless Steel (S.S) to ensure both structural strength and biocompatibility.
Is the product delivered sterile?
Yes, the products are provided in sterilized PE bags and carton packaging, meeting medical safety standards.
What is the shelf life or valid time for these instruments?
The sterilized instruments have a valid shelf life of 3 years from the date of production.
Does the system comply with international quality standards?
Yes, the production process is certified under CE and ISO9001 quality management systems.
Can this be used for pediatric patients?
This specific model (1015b-a) is categorized for adult use, though other specifications may be available for different patient groups.

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