Medical Devices

*Cernex Pharma verifies valid conformity markings and technical documentation.

Quality & Compliance

Medical Devices & Diagnostic Equipment Supply


Every medical device is verified for valid CE or UKCA marking, accompanied by a Declaration of Conformity

Cernex Pharma extends its sourcing capability beyond pharmaceuticals to encompass CE-marked and UKCA-marked medical devices, surgical consumables, and diagnostic equipment. We supply healthcare facilities with products that meet European and UK conformity assessment requirements, ensuring that every device is traceable to its manufacturer and supported by valid declaration of conformity.

Our medical devices service addresses the procurement needs of hospitals, clinics, and diagnostic centres requiring reliable access to regulated medical technology.

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Technical Capabilities

Diagnostic Equipment

We procure diagnostic devices, including point-of-care testing equipment, imaging consumables, and laboratory reagents subject to verification of manufacturer conformity assessment and intended-use documentation.

CE/UKCA-Marked Consumables

We supply sterile and non-sterile medical consumables including syringes, catheters, wound care products, and infusion sets that carry valid CE or UKCA marking and conform to applicable Medical Device Regulation (MDR) requirements.

Device Registration Support

Where destination countries require local medical device registration, we provide manufacturer documentation packs to support registration applications by the importing entity.

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Our Services

Pharmaceutical Wholesale

Specialist Sourcing Service

International Procurement

Medical Devices Supply

Humanitarian & Institutional Supply

Unique Device Identification (UDI)

We support traceability through batch/lot number tracking and, where available, Unique Device Identification (UDI) capture. This enables rapid identification and recall management if safety issues emerge.

At Cernex Pharma, we maintain communication channels with device manufacturers to facilitate vigilance reporting and field safety corrective actions (FSCA) .

+44 (0) 33 3123 4558

enquiries@cernexpharma.co.uk

Unique Device Identification (UDI)

We support traceability through batch/lot number tracking and, where available, Unique Device Identification (UDI) capture. This enables rapid identification and recall management if safety issues emerge.

At Cernex Pharma, we maintain communication channels with device manufacturers to facilitate vigilance reporting and field safety corrective actions (FSCA) .

+44 (0) 33 3123 4558

enquiries@cernexpharma.co.uk