No-Obligation Quotation

Send Us Your Requirements
Get a Detailed Quote

We review every RFQ within 24 business hours and respond with pricing, lead time, and available certifications — no obligation.

ISO 13485:2016
FDA 510(k) Registered
CE (EU MDR)
13+ Years Manufacturing
120M Pieces Annual Capacity

Before You Fill Out the Form

We've been doing this since 2012. The buyers who get the most useful first quote are the ones who give us three things: the product type, the quantity, and the destination market. Everything else — packaging format, certification requirements, private-label specs — we can work through in the follow-up.

If you're not sure which product fits your market, tell us the end channel (hospital procurement, retail pharmacy, government tender, private label) and the regulatory framework you're selling into. We'll recommend the right SKU and spec.

EU Buyers — Important Note

Most buyers sourcing for the EU for the first time don't realize the MDR documentation requirements have changed significantly since 2021 — we've walked a lot of European customers through this before they placed their first order.

For the Best First Quote, Include:

  • 1
    Product type (surgical, N95, disposable, PPE)
  • 2
    Approximate quantity needed
  • 3
    Destination market / country

Everything else — packaging, certifications, private-label specs — we can work through together after the initial quote.

eztio quote process — from RFQ submission to detailed pricing response

Request a Quote

Complete the form below with your requirements. We'll respond with pricing, lead time, and certification details within 24 business hours.

Required Information

Fields marked with * are required

Our standard MOQ is 50,000 pieces for most SKUs. Custom configurations may require higher minimums.

Optional Details

These help us provide a more accurate first response

Helps us confirm which certifications apply

Share it and we'll spec accordingly

No obligation. We'll review your requirements and respond within 24 business hours.

Response Time

Every RFQ is reviewed and responded to within 24 business hours with pricing, lead time, and certification details.

Standard MOQ

50,000 pieces for most SKUs. Custom configurations may require higher minimums — we'll confirm in our response.

Certifications

  • ISO 13485:2016
  • FDA 510(k) Registered
  • CE (EU MDR)
View all certifications

Prefer to Talk First?

If you'd rather discuss your requirements before submitting a formal RFQ, reach out directly.

Contact Us
Your Next Steps

What Happens After You Submit

1

We Review Your Requirements

Within 24 business hours, a member of our team reads your RFQ and confirms we can fulfill it.

2

We Prepare Your Quotation

Pricing, lead time, available certifications, and packaging options based on your destination market.

3

You Receive the Quote by Email

With full product specs, test report references, and any documentation relevant to your import process.

4

We Answer Your Follow-Up Questions

Most buyers have 2–3 rounds of questions before confirming an order; that's normal and expected.

Sharpen Your Quote

What to Include for the Most Accurate Quote

For a first-round quote that's actually useful, the more of these you can provide, the better.

Don't have everything?

You don't need all of these to get started. A product type and quantity gets us to a ballpark. The rest sharpens the number.

Buyer preparing medical mask quote request documentation

Product Type & Configuration

3-ply surgical, N95, 4-ply disposable, etc.

Quantity

Approximate is fine; we'll confirm MOQ if it applies.

Destination Market

Determines which certifications and documentation we prepare.

Packaging Format

Bulk clinical, retail box, private-label (if applicable).

Certification Requirements

FDA, CE, ASTM level, EN 14683 class, or equivalent.

Delivery Timeline

Especially if you're working toward a tender or seasonal deadline.

Market-Ready Documentation

Certifications Covering Your Key Markets

The certifications on our products aren't decorative — they're the entry ticket to the markets you sell into.

ISO 13485:2016

Medical device QMS, required for most institutional and hospital procurement.

ISO 9001:2015

General quality management system certification.

CE (EU MDR)

European market access; full technical file available for your importer of record.

FDA 510(k) Registered

US market clearance; import documentation prepared with every shipment.

SGS

Third-party audit and testing verification.

If your market requires documentation we haven't listed, ask. We've exported to North America, Europe, the Middle East, Southeast Asia, and Africa — the paperwork requirements vary, and we've handled most of them.

Prefer to Talk First?

Not every sourcing conversation starts with a form. If you have questions before you're ready to submit an RFQ — about product specs, certification coverage, MOQ flexibility, or OEM options — reach us directly.

Phone / WhatsApp
+86 190 0636 0409
Business Hours
Mon–Fri, 9:00–18:00 CST (UTC+8)

We typically respond to direct emails within the same business day.

Just have questions? Contact us instead

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