Disposable Anesthesia Breathing Corrugated Circuit for Ventilator with ISO, CE, FDA

Name: Disposable Anesthesia Breathing Corrugated Circuit for Ventilator with ISO, CE, FDA
Brand: Hangzhou Trifanz Medical Device Co., Ltd.
SKU: 1935637111

Zhejiang, ChinaHangzhou Trifanz Medical Device Co., Ltd.

US$1.70-4.50

100 Pieces

Sample price:US$4.50/piece.Request sample

Product profile

Customization

Available

Material

PVC, Polymer

Feature

Disposable

Model NO.

Adult, Pediatric, Neonatal

Certification

ISO13485, FSC, China FDA

Ethylene Oxide Sterilization

Application

Hospital

Group

Adult, Pediatric, Neonatal

Logo Printing

Without Logo Printing

Delivery Time

3-30days

OEM/ODM

Available

Stylet

Optional

Type

Surgical Supplies Materials

Properties

Medical Materials & Accessories

Size

1.2#1.5#1.6#

Color

Transparent

OEM

OEM Service Accepted

Usage

Single-Use

Packaging

1 Piece/Bag

Keyword

Disposable Breathing Circuit

Sample

Sample Offered

Place of Origin

Zhejiang, China

Transport Package

Paper Plastic Plain Pouch, Carton

Specification

size adult, size pediatric, size neonate

Trademark

Trifanz

Origin

China (Mainland)

HS Code

9019200000

Production Capacity

10000/Day

Company profile

Hangzhou Trifanz Medical Device Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/Factory, Trading Company, Group CorporationExport Year: 2020-03-17Nearest Port: Shanghai, Ningbo, YiwuAverage Response Time: ≤3.76hTerms of Payment: LC, T/T, PayPal, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF, FAS, CIP, CPT, FCA, EXW, Others

AI-Powered supplier vetting

SummaryHangzhou Trifanz Medical Device Co., Ltd. is identified as a China-based limited company and factory/manufacturer operating in medical devices, particularly anesthesia, respiratory, and catheter products. The supplier reports ISO 13485 and ISO 9001 certification, five production lines, 6–10 R&D engineers, and 6–10 quality-control staff. It states that OEM/ODM services are available and describes export capability, with exports representing 51%–70% of sales and self-operated import/export rights. The evidence supports a relevant manufacturing profile, documented quality systems, production infrastructure, and customization availability. However, the provided information does not sufficiently establish after-sales service capability, financial credibility, or verified customer cases. The supplier’s claimed certificates beyond ISO certifications and its product and market experience are not independently substantiated in the slices.

Supplier typeThe supplier is identified as a limited company, trading company/manufacturer/factory, and group corporation in one record, while another record classifies it as a factory. Its stated operations cover R&D, production, and sales of medical anesthesia and respiratory products, with Hangzhou, China locations consistently reported.

CertificationsThe supplier explicitly reports ISO 13485 and ISO 9001 management-system certifications. It also claims ZFDA, FSC, SGS, and COA documentation, but the slices do not provide certificate numbers, validity dates, or independent verification for those additional claims.

R&D capabilityThe supplier describes itself as an innovation-oriented medical-device enterprise engaged in R&D and reports 6–10 years of total R&D engineer experience. Its stated focus includes developing anesthesia and respiration products, which supports relevant technical development capability, although no patents, laboratories, or specific innovations are provided.

Production capacityThe supplier is classified as a factory/manufacturer and reports five production lines, 6–10 quality-control staff, and a factory location in Hangzhou. Its described manufacturing scope includes disposable anesthesia and breathing products and medical catheters, providing explicit evidence of relevant production infrastructure.

Customization capabilityThe supplier explicitly states that OEM/ODM services are available and that it can provide other certificates according to a customer’s market. The slices do not define customization limits, tooling capability, minimum order requirements, or validation procedures.