Twelve questions worth asking before you appoint a contract manufacturer, answered directly. Every statement can be checked during a factory audit.
Check four things: qualifications, cleanroom class, quality control and openness. Ask whether the factory holds a Class I medical device manufacturing filing, whether it runs a Class 100,000 cleanroom, whether it supplies a third-party report for every batch, and whether it will let you audit the site. Our factory meets all four and welcomes on-site verification.
A hygiene product production licence, a Class I medical device manufacturing filing and a disinfection product production hygiene licence. Together they allow maternal/baby, medical and disinfection products to be made legally within one production system, so you do not need to change suppliers when your range expands into medical or disinfection categories.
ISO9001 (28826Q00086R0S3) and ISO14001 (28826E00053R0S3) are published with certificate numbers, validity dates and bilingual scans on our certifications page. ISO13485, CE and FDA export documentation items are listed as documentation to be confirmed until the originals are supplied; we do not claim them as certified.
A Class 100,000 cleanroom with a Class 10,000 laboratory. UV, ozone, ethylene oxide (EO) and irradiation sterilisation are matched to the product category rather than applied uniformly.
15 fully automatic lines, six of them servo high-speed at 1,500 pads per minute per line. Export orders, e-commerce promotion orders, annual chain contracts and hospital tenders can run in parallel, and peak capacity can be reserved in advance.
OEM means we produce to your sample or specification and apply your label. ODM means we jointly develop from specification definition through topsheet and core selection, grammage tuning and packaging design. Both are supported, including small trial orders.
Yes. Most customers start with a trial order to confirm sample quality and market feedback before scaling. Exact MOQ depends on category, size and packaging and is agreed in the contract.
15-20 days for standard orders, with pre-shipment inspection supported. Reserve capacity one to two months ahead of peak season for large promotion or tender volumes.
A third-party test report accompanies every batch. The Class I medical device filing, licence documents and batch reports can be provided for hospital and institutional onboarding review; see the certification register for what is currently published.
Yes. Bag or box format, colour printing, logo, barcodes and compliance labels are produced to the target market. We hold self-operated import/export rights and ship directly from Qingdao Port.
Twelve lines: disposable nursing pads, baby underpads, maternity and adult care pads, medical underpads, baby diapers and adult pants, postpartum/medical sanitary napkins, breast milk storage bags, medical paper and wipes, disinfection products, newborn T-shape diapers, maternity kits and sanitary napkins.
Yes. On-site audits and live video factory tours are welcome. The factory is at No.778 Mingyue Road, Huangdao District (West Coast New Area), Qingdao, near Qingdao Port. Please call +86 13869876727 ahead of your visit to arrange reception and a workshop tour.
Our sales team answers within 24 hours on working days (Mon-Sat 08:00-18:00 GMT+8). Send an enquiry → or call / WhatsApp +86 13869876727. For category specifications, see the full product catalogue →.
Tell us the category, size, quantity and target market. Phone / WhatsApp: +86 13869876727 · We reply within 24 hours on working days.
