Popular New Model CE-Approved Medical Grade Material Home Use Low Noise DC Compressor Nebulzier for Asthma

Description

Shenzhen Fitconn Technology Co.,ltd was founded in 2012 . It is a comprehensive enterprise dedicated to the research and development, manufacturing, sales and after-sales service of household medical products. The products cover nebulizer (compressor nebulizer, DC Compressor nebulizer and Mesh nebulizer), anti-decubitus air mattress, oximeters, fetal doppler, blood pressure monitors, etc. The business covers more than 150 countries around the world, with an average annual service of more than 2,000,000 family. Fitconn adheres to the concept of create health by heart, and is committed to improving the diversification of atomization methods, let’s households medical products and modern medical technology can benefit thousands of families around the world, with respect, tolerance, integrity, efficiency, innovation and persistence as core values, Integrate superior resources, take innovation as the source of development, and take science and technology as the foundation of success, and strive to provide each consumer with more professional, advanced and safer medical products. Fitconn has the class II medical device production qualification and over 50 patents , the company has passed the 13485 quality system certification, and some products have passed the EU CE and FDA certification

Fitconn CDC500: Compliance You Can Verify, Not Just Claims You Have to Trust

Anyone who has sourced medical devices knows the routine. A supplier lists CE, RoHS, ISO 13485 in the product attributes. The buyer nods, assumes it is real, and moves on. Nobody asks for the certificate number. Nobody checks the validity dates. And occasionally — more often than the industry likes to admit — the certification turns out to be expired, mismatched to the wrong product family, or issued by a body that no longer holds notified status.

The Fitconn CDC500 takes a different approach. Its MDR certificate is FI26/1008022, valid from 16 April 2025 through 15 April 2031. Its RoHS certificates are CANEC24026653801 and CANEC24026641701, both running through late 2029. Its 93/42/EEC compliance extends to 30 December 2028. These are not badges on a marketing page. They are traceable documents with numbers a compliance officer can verify independently — and that transparency tells you more about the manufacturer than any specification ever could.

The Smallest Compressor in the Catalog

At 136 by 86 by 56 millimeters, the CDC500 is the most compact DC compressor nebulizer Fitconn produces. To put that in perspective, it is smaller than a paperback novel and roughly the footprint of a standard smartphone lying flat with a little extra height. This is not a mesh device trading power for size. It is a genuine piston-driven compressor, miniaturized without abandoning the pressure architecture that makes compressor nebulizers clinically dependable.

The compressor sustains a 40 to 80 KPA operating pressure range with an output gas flow of ≥3.5 L/min, driving nebulization at a steady ≥0.2 mL per minute. Median particle size lands at ≤3.8 micrometers with a ±25% tolerance, placing the aerosol squarely in the bronchial and bronchiolar deposition zone where the majority of asthma and respiratory medications achieve peak absorption.

Type-C Power in a Medical Device

The CDC500 charges and operates through a USB Type-C connection — the same cable that powers phones, laptops, tablets, and virtually every modern portable electronic device. This matters more than it might initially appear. A medical device that uses a proprietary power brick becomes unusable the moment that brick is lost, damaged, or left behind. A medical device that runs on Type-C is powered by whatever cable is nearest.

The unit accepts AC 110–220V at 50/60Hz with an input power draw of just 18VA — universal voltage that works in every market without a transformer, and a power consumption low enough that the device can run from a modest power bank. For patients who travel, for clinics in regions with unstable grid supply, and for anyone who has ever discovered their nebulizer adapter missing at the worst possible moment, this is a meaningful practical advantage.

Fifty Decibels and an 8 mL Cup

The CDC500 operates at ≤50 dB(A) — below the sound level of ordinary conversation and comfortably within range for bedside, office, or shared-space use. For a mechanical compressor rather than a silent piezoelectric mesh, achieving this noise floor requires deliberate engineering in the motor mount, housing damping, and airflow path.

The 8 mL medication cup exceeds the 3–5 mL capacity typical of portable units, supporting longer treatment cycles without interruption for refilling. The residual volume stays under 1 mL, keeping medication waste low across repeated daily sessions. For chronic patients running two or three treatments per day, that efficiency compounds into measurable savings over a year of therapy.

Environmental Tolerance and Build Integrity

The CDC500 is rated for operation across 5°C to 40°C, relative humidity from 15% to 80%, and atmospheric pressure from 70.0 to 106.0 KPA — a range that covers virtually every inhabited indoor environment, from humid tropical clinics to dry high-altitude households. The plastic housing in white is durable and easy to sanitize. The device carries Class II medical instrument classification and complies with GB/T18830-2009 safety standards.

The Manufacturer Behind the Certificates

The CDC500 is built by Shenzhen Fitconn Technology Co., Ltd. — 21 years in medical device manufacturing, a 4.9 out of 5 store rating, a 23% reorder rate, and the number one ranking among household medical device factories on its platform. The company is TÜV verified, holds ISO 13485 quality management certification, and manufactures under CE, MDR EU, and 93/42/EEC compliance.

Fitconn operates a full pre-production sampling process before every mass run and conducts final inspection before shipment. The company accepts third-party inspection, offers OEM and ODM service, and grants exclusive territory rights to major clients. Some models carry proprietary design patents. This is a factory with a documented process, not a workshop assembling white-label units to order.

Who Should Carry This Product

The CDC500 is the right choice for a distributor entering regulated European markets where MDR documentation is not optional and expired certificates halt shipments at customs.

It is also the right choice for a retail channel where compact form factor and universal charging drive purchase decisions — travel pharmacies, airport health retail, and online storefronts serving customers who want a nebulizer that fits in a laptop bag and charges from the same cable as everything else they own.

Customized logo, packaging, and graphic design are available at 1,000 pieces MOQ, making the CDC500 a viable platform for private-label brands that need certified compliance without building their own regulatory infrastructure.

The Final Word

The Fitconn CDC500 competes on something most nebulizers cannot: verifiable proof. Anyone can print CE on a box. only a manufacturer confident in its documentation does that voluntarily. Combined with the smallest compressor footprint in the Fitconn range, Type-C universality, and a sub-50 dB noise floor, the CDC500 is a product that answers the questions serious buyers actually ask before the buyer has to ask them.