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Innovative Uterine Stents for Effective Bleeding Control Solutions
Negotiable
500 Sets

Product profile

Customization

Available

Material

Silicone

Disinfecting Type

EOS

Model NO.

FZ-10, FZ-20

Safety Standard

ISO19330

Instrument Classification

Class III

Size

5ml, 8ml

Quality Certification

CE

Shelf Life

3 Years

Properties

Personal Safety

Stock

Yes

Trademark

ABLE

Origin

Guangdong

Key features

Physiological Design: Inverted triangle structure conforms to uterine morphology for effective cavity support and adhesion prevention.
High Biocompatibility: Made of soft silicone with good biocompatibility and high saccule tolerance for patient comfort.
Painless Operation: Easy to place and remove quickly, ensuring the patient experiences no pain during the procedure.
Wide Applicability: Suitable for a wide range of patients, including those with surgical damage to the uterus.
CE Certified Quality: Class III medical device with CE certification and ISO19330 safety standard compliance.
Customizable Options: Disinfecting type is customizable to EOS; available in 5ml and 8ml sizes.

Company profile

Guangdong Baihe Medical Technology Co., Ltd.
High Repeat Buyers ChoiceYears of Export Experience
Business Type: Manufacturer/FactoryExport Year: 2001-10-01Nearest Port: huangpu, shenzhen, shanghaiAverage Response Time: ≤5.28hTerms of Payment: LC, T/T, PayPal, etc.International Commercial Terms(Incoterms): FOB, EXW, CIF, Others

AI-Powered supplier vetting

SummaryThe supplier demonstrates broad medical-device manufacturing and sales scope, including multiple device classes, protective equipment, catheters, dialyzers, blood lines, and related products. It offers OEM, ODM, flexible customization, and customization from designs or samples, and reports new product development within the past year. Production-related strengths include valid contracts with associated subcontractors, in-stock capability, one-month average lead times in both peak and off-season, and 100 quality assurance and quality control inspectors. Service management procedures, complaint-handling procedures, and corrective and preventive action procedures are documented and followed. The supplier also supports overseas agents or branches, training services, and has participated in an offline trade show. However, it has no overseas warehouse or showroom, no available SDK, and the provided information does not establish formal certifications, detailed customer cases, or sufficient evidence to assess...
Supplier typeThe supplier is positioned as a medical-device manufacturer and seller, with stated capabilities covering Class I, II, and III medical-device production or management, protective equipment, masks, and sanitary or single-use medical supplies. This indicates a broad, regulated healthcare-product business scope rather than a general trading-only profile.
After-Sales capabilityThe supplier has written procedures and implementation records for customer complaint handling, corrective and preventive actions, and broader service-capability assessment. It also provides overseas-agent or branch support and training in Hong Kong, Singapore, Turkey, India, and Pakistan, although no overseas warehouse or showroom is available.
R&D capabilityThe supplier reports new products within the past year, offers ODM services and multiple design-development options, and uses ERP, OA, CRM, and SAP systems for digitalized operational management. However, it has no available SDK, so software-development integration capability is specifically limited.
Production capacityThe supplier reports valid manufacturing contracts with every associated subcontractor, in-stock capability, one-month average lead times in both peak and off-season, and 100 quality assurance and quality control inspectors. Its stated product and facility information includes catheters, dialyzers, blood lines, and an ethylene oxide sterilizer production facility, supporting a substantial manufacturing operation.
Customization capabilityThe supplier explicitly provides flexible, minor, and full customization, including customization from customer designs and samples. It also offers ODM services, indicating capability beyond standard catalog supply.

Product Q&A

Q:What are the available sizes for the uterine stent?
A:
The product is available in two sizes: 5ml (Model FZ-10) and 8ml (Model FZ-20).
Q:Is the uterine stent customizable?
A:
Yes, the disinfecting type can be customized to EOS. Other specifications like size are also available options.
Q:What is the shelf life of the product?
A:
The shelf life of the uterine stent is 3 years.
Q:What certifications does the product have?
A:
The product holds CE certification and meets the ISO19330 safety standard. It is classified as a Class III instrument.
Q:What is the lead time for production?
A:
The average lead time is one month for both peak season and off-season.

Send Inquiry

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