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Breathing Exercise Device for Lungs, Lung Exerciser, Lung Exerciser Device, Lung Exercise Treatment, Respiratory Muscle Trainer, Breathe Exercise Device for Lun
US$2.50-5.80
100 Pieces

Product profile

Customization

Available

Brand Name

Kealor/OEM

Certificate

CE ISO13485 GMP

Model NO.

Breathing Exerciser

Sterilization Method

Eo

Shelf Life

5years

Package Type

Sterile Package, Packed by Blister

Trademark

KEALOR

Origin

China

HS Code

9018310000

Production Capacity

500000PCS/Year

Key features

5-Year Shelf Life: Valid for 5 years when stored in stipulated conditions.
CE and ISO13485 Certified: Meets international medical device safety and quality standards.
OEM Branding Available: Supports custom branding for medical grade PVC/TPU devices.
Flow Rate Indicator: Visual guide ensures optimal inhalation speed and control.
High-Quality Material: Made of break-resistant plastic with no peculiar smell.
Easy to Clean Design: Removable tube and mouthpiece allow thorough hygienic maintenance.
Built-in Filter Cotton: Integrated filter ensures cleaner breathing during therapy.
5000ml Volume Capacity: Large measurement range suitable for deep breathing training.

Company profile

Changzhou KEALOR International Co., Ltd.
High Repeat Buyers ChoiceQuality AssuranceRaw-Materials TraceabilityQA/QC Inspectors
Business Type: Manufacturer/FactoryExport Year: 2025-02-18Nearest Port: shanghaiAverage Response Time: ≤15hTerms 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

SummaryKealor presents evidence of established medical and aesthetic manufacturing capabilities, holding ISO 13485, ISO 9001, and GMP certifications, reporting 50 quality-control staff, annual output above the stated threshold, and experience supplying well-known brands. It offers OEM, ODM, and multiple customization options, with raw-material traceability and documented inspection instructions. However, the evidence is inconsistent regarding technical resources: one slice identifies only one R&D engineer and no quality-control test equipment, while another reports 11–20 years of total R&D engineer experience. The supplier lacks 3D software, SDK, overseas warehouses, overseas showrooms, overseas agents or branches, and offline trade-show participation. After-sales technical support is indicated, but formal service-management procedures are absent. Financial records are referenced for several years, but the provided data does not disclose financial performance details. Customer cases are not specifically identified.
Supplier typeThe supplier is explicitly described as not being a professional technical supplier, while its company description focuses on solutions for medical and aesthetic applications. Its certifications and manufacturing indicators support classification as a medical/aesthetic product manufacturer rather than a dedicated technical-services provider.
CertificationsThe supplier reports holding ISO 13485, ISO 9001, and GMP certifications. These explicitly demonstrate certifications covering medical-device quality management, general quality management, and good manufacturing practices.
Production capacityProduction-related evidence includes annual output above the stated threshold, in-stock capability, raw-material traceability, one quality-control inspector, random finished-product inspection, and inspection instructions that are uniformly followed. The supplier has no quality-control test equipment reported in one slice, and manufacturing-contract status is unknown, so production scale is demonstrated but process depth and capacity assurance are only partially evidenced.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, full customization, minor customization, and flexible customization, together with OEM and ODM services. These repeated capabilities indicate broad product customization support, despite the absence of 3D software design services.

Product Q&A

Q:What is the shelf life of the device?
A:
The device has a validity period of 5 years when stored in stipulated conditions.
Q:Is OEM service available for this product?
A:
Yes, OEM branding is available for the medical grade PVC/TPU devices.
Q:What certifications does the product have?
A:
The product holds CE, ISO13485, and GMP certifications.
Q:How should the device be stored?
A:
Store indoors at normal temperature with humidity no more than 75%, avoiding corrosive gases, direct sun, rain, and snow.
Q:What is the recommended usage time?
A:
It is recommended to use the device for 5-10 minutes every day for better effects.

Send Inquiry

*To:Changzhou KEALOR International Co., Ltd.Changzhou KEALOR International Co., Ltd.
*Content:
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