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Icen Low Foreign Body Reaction Hernia Repair Mesh Fixation Device Plga Absorbable Tacker
US$130.00-180.00
1 Piece

Product profile

Customization

Available

Application

Surgery

Material

Plga

Model NO.

IN-P7

Feature

Disposable

Certification

CE, ISO13485

Product Name

Absorbable Tacks for Soft Tissue Repair

Absorbable

Yes

Nail Material

Plga

Packing Specification

1 Set/Box

Specification

10 -30tacks

Trademark

ICEN

Origin

China

Key features

Low Foreign Body Reaction: PLGA material degrades into glycolic and lactic acid, minimizing residue in patients.
Complete Shape Retention: Maintains full shape for 26 weeks post-implantation with only 15% shear strength loss.
Safe Blunt Nail Design: Blunt nail tail design ensures safety for both doctors and patients during surgery.
One-Handed Operation: Ergonomic design allows for easy, one-handed operation in laparoscopic and open surgeries.
Wide Specification Range: L type (360mm) and S type (215mm) available with 5-32 nails to meet various surgical needs.
CE & ISO13485 Certified: Product holds CE and ISO13485 certifications, meeting Class III instrument safety standards.
Disposable & Sterile: Single-use disposable design ensures hygiene and prevents cross-contamination.
1-Year Warranty: Comprehensive 1-year warranty coverage with online technical support for after-sales service.

Company profile

ICEN Medical Equipment Limited
High Repeat Buyers ChoiceMulti-language PioneerIn-stock CapacityFast Delivery
Business Type: Manufacturer/FactoryExport Year: 2017-10-01Average Response Time: ≤10.24hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DAT, FAS, DDP, DAP, CIP, CPT, Others, FCA

AI-Powered supplier vetting

SummaryICEN Technology Company Limited is identified as a China-based manufacturer/factory and limited company, although another record describes it as a trading company. It offers a broad range of medical equipment and reports OEM service for popular brands. The supplier holds ISO 9001 certification, has 6–10 quality-control staff and 6–10 R&D engineers, operates two production lines, and reports lead times within 15 workdays in both peak and off-peak seasons. R&D documentation is available for audit, but no SDK is available and the supplier reports zero R&D patents. It has inventory capacity and provides training, but lacks overseas agents or branches, overseas warehouses, overseas showrooms, and documented manufacturing-capacity contracts with affiliated subcontractors. Financial records are referenced for 2022–2024, but no financial performance details are provided. Customer project experience is described, including hospital design, equipment installation, and after-sales service, but no named customer...
CertificationsThe supplier reports ISO 9001 certification. An audit was conducted by BV, with a report period from 2025-10-23 to 2026-10-22, but the supplied audit result is recorded as 0 and no further interpretation or certification details are provided.
After-Sales capabilityThe supplier states that it provides equipment installation and after-sales service and lists training among its overseas service offerings. However, it has no overseas agents or branches, no overseas warehouse or showroom, and reports service coverage in zero countries, indicating that overseas service infrastructure is limited.
R&D capabilityThe supplier has 6–10 R&D engineers, uses PS and CAD software, operates production-line equipment, and can provide design input, output, review, verification, and validation documentation for audit. However, it reports zero R&D patents and no available SDK, so evidence supports operational R&D capability but not strong proprietary innovation.
Production capacityThe supplier operates two production lines, has 6–10 quality-control staff, reports lead times within 15 workdays during both peak and off-peak periods, and maintains in-stock capacity. Nevertheless, it has no valid manufacturing-capacity contract with affiliated subcontractors, which limits visibility into extended production resources.
Customization capabilityOEM service for popular brands is explicitly reported, and the supplier maintains R&D documentation covering design inputs, outputs, reviews, verification, and validation. These records support customization and product-development coordination, although no specific customized product examples are provided.

Product Q&A

Q:What is the degradation time of the absorbable nail?
A:
The nail degrades in vivo after 52 weeks, with glycolic acid and lactic acid being absorbed and metabolized by tissues.
Q:What materials are used for the absorbable tacks?
A:
The absorbable nail is made of poly-L-lactide-glycolide (PLGA).
Q:What are the available specifications for L type and S type?
A:
Both L type (360 mm) and S type (215 mm) contain 5-32 nails to meet various surgical needs.
Q:Is the product suitable for laparoscopic surgery?
A:
Yes, it is suitable for fixing hernia mesh and other soft tissue repair materials in both laparoscopic and open surgery.
Q:What certifications does the product hold?
A:
The product has CE and ISO13485 certifications and is classified as a Class III instrument.

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