Quality and certification
Certified management systems, documented batch release and independent barrier testing behind every carton we ship.
Approved for regulated markets
Papers ready for customs and tenders
Our facilities operate under ISO 9001 and ISO 13485 quality management systems, with products carrying CE marking and registration with the US FDA.
We supply certificates of analysis, free-sale certificates, sterilisation records and material declarations with commercial shipments.
Technical files and test reports are available to qualified buyers for tender submission and regulatory review.
Seven checks before anything leaves the line
Pinhole Control
Every glove passes electronic air inspection and seven separate quality checks before release. Final pinhole AQL is held below 1.0 against an industry standard of 1.5.
Chemotherapy Drug Barrier
Independently tested in the United States against 18 antineoplastic agents in line with ASTM D6978, for safe handling of cytotoxic drugs.
Free From Thiuram & DPG
No thiuram or DPG accelerators are used, substantially reducing the risk of Type IV contact allergy for long-term wearers.
Electron Beam Sterilisation
Precise dose and dwell control, with no ethylene oxide residue and no environmental burden — safer for patients and staff.
Controlled Grip Strength
A five-level grip index is used as an internal control so every product matches its intended clinical use, from microsurgery to orthopaedics.
Verified Barrier Performance
ASTM F1671 virus penetration, ASTM F1670 blood penetration and SATRA chemical permeation testing across eight acid and base solutions.
Independent verification, not in-house optimism
Barrier performance is confirmed by independent laboratories: ASTM F1671 for viral penetration, ASTM F1670 for blood penetration, and SATRA protocols for chemical permeation across eight acid and base solutions.
Chemotherapy-drug resistance is tested against 18 antineoplastic agents in line with ASTM D6978 at a US laboratory.
Antiviral performance of our KBD glove range has been evaluated by the Wuhan Institute of Virology, showing physical inactivation of SARS-CoV-2 at 94.87% and HIV at 99.7%.
Controlled production conditions
Production runs under controlled cleanroom conditions with filtered air, designated gowning routes and continuous monitoring of temperature and humidity.
Gloves are sterilised by electron beam with logged dose control, avoiding ethylene oxide residues on the finished product.
Finished goods are quarantined pending release and held under documented storage conditions before dispatch.
Request samples or a quotation
Tell us the items, sizes, packing and quantity you need. Samples can be arranged for qualified buyers, and OEM packing is available from opening order quantities.
Talk to us about your requirement
Send us your product list, target specification and destination market. We will reply with pricing, sample availability, lead time and the documents you need for import clearance.
We welcome enquiries from distributors, hospital groups, private-label brands and OEM partners.
WhatsApp: @gophersource
Office: No. 87 Kechuang 6th Street,
Beijing Economic-Technological Development Area,
Beijing, China
Frequently asked questions
What disposable gloves does Gopher Source supply?
Surgical gloves in powder-free and powdered natural latex, examination gloves in latex, nitrile and PVC, and protection gloves in nitrile and PVC – alongside infusion and IV therapy consumables and monitoring accessories.
Which quality standards are your gloves tested to?
Independent barrier testing covers ASTM F1670 for blood penetration, ASTM F1671 for virus penetration, ASTM D6978 for chemotherapy drug permeation across 18 antineoplastic agents, and SATRA chemical permeation testing across eight acid and base solutions.
What certifications do you hold?
Our facilities operate under ISO 9001 and ISO 13485 quality management systems, with products carrying CE marking and registration with the US FDA.
Do you provide documentation for customs clearance and tenders?
Yes. Certificates of analysis, free-sale certificates, sterilisation records and material declarations are supplied with commercial shipments. Technical files and full test reports are available to qualified buyers for tender submission and regulatory review.
How is pinhole quality controlled?
Every glove passes electronic air inspection and seven separate quality checks before release. Final pinhole AQL is held below 1.0, against an industry standard of 1.5.
How do I request a quotation or samples?
Send your product list, target specification and destination market through the form on our contact page or by email. We reply within one business day.