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Minimally Invasive Spinal Fixation System for Scoliosis Surgery with ISO Certification
US$85.00
1-4 Pieces
US$82.00
5-9 Pieces
US$80.00
10+ Pieces

Product profile

Type

Misfix 5.5 System

Syringe

Misfix 5.5 System

Blood Sampling Needle

Misfix 5.5 System

Model NO.

MisFix 5.5 System

Breathing Pattern

Misfix 5.5 System

Animal Anesthesia Machine Control Method

Misfix 5.5 System

Certification

FDA, CE

Disinfection

Disinfection

Color

Misfix 5.5 System

Application

Misfix 5.5 System

Material

Misfix 5.5 System

Transport Package

PE Film

Specification

1pcs

Trademark

XC MEDICO

Origin

China

Key features

Minimized Profile Design: Slim design reduces tissue disruption and facilitates easy insertion during surgery.
High-Strength Materials: Constructed from titanium or cobalt-chromium for durability and biocompatibility.
Mechanically Stable: Bent rod fits tightly with no gaps ensuring continuous and reliable force transmission.
Precise Reconstruction: Controlled distraction and reduction for precise restoration of disc height and alignment.
Sub-Micron Accuracy: Manufactured using CNC Turning, Milling, and Wire EDM for high precision.
Comprehensive Traceability: Mechanical tests archived for over 3 years with full process traceability.
FDA and CE Certified: Product holds FDA and CE certifications for international compliance.

Company profile

Xc Technology Co., Ltd.
In-stock CapacityFast DeliveryRaw-Materials TraceabilityQuality Assurance
CertifiedBusiness Type: Trading Company CertifiedCustomization Options: Minor Customization CertifiedExport Year: 6 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤6.82h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryXC Medico is identified as a trading company serving the health and medicine sector, with orthopedic instruments as a key product area. The supplier reports 18 years of orthopedic experience, certified production lines and warehouses, raw-material traceability, and 100% finished-product inspection, although inspection is performed by packing staff and only one quality inspector is reported. Service infrastructure is limited: no overseas warehouses, showrooms, agents or branches, and no offline trade-show participation. Formal service procedures, corrective/preventive-action records, and complaint-handling procedures are not provided. Innovation evidence is weak, with no new products in the past year, no ODM, OEM for popular brands, or SDK. Minor customization is available. Certification is mentioned, but specific certificates are not identified. Customer cases are not documented.
After-Sales capabilityThe supplier claims technical support covering preoperative planning, intraoperative assistance, and postoperative traceability and complication management. Against this, it reports no written service procedures or records, no formal corrective/preventive-action mechanism, no documented complaint-handling process, and no overseas warehouses, showrooms, agents or branches; therefore, structured and geographically accessible after-sales capability is not demonstrated.
R&D capabilityThe supplier describes experienced engineers and product development and innovation, but reports no new products during the past year, no ODM service, no OEM for popular brands, and no available SDK. The explicit recent innovation and development offerings therefore indicate a deficiency.
Production capacityThe supplier states that it operates certified production lines and warehouses, has a 668.0 m² manufacturing plant, provides raw-material traceability, and conducts 100% finished-product inspection. However, finished products are checked by packing staff and only one quality inspector is reported; production capability is supported by facility and control claims, but its scale and robustness are only partially evidenced.
Customization capabilityThe supplier explicitly offers minor customization. This confirms some customization capability, but the evidence does not show advanced engineering customization, extensive configuration options, or full OEM/ODM support.

Product Q&A

Q:What materials are used for the system?
A:
The system uses titanium or cobalt-chromium, conforming to GB/T 13810-2017 standards.
Q:What surgeries is this system indicated for?
A:
It is indicated for minimally invasive surgery of fractures, degeneration, spondylolisthesis, and revision.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 piece.
Q:What are the payment terms?
A:
We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments.
Q:How long is the lead time?
A:
The average lead time is within 15 workdays for both peak and off-peak seasons.

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