EN

Laboratory & diagnostic packaging: Produced in an automated cleanroom

We develop and manufacture primary and secondary packaging for laboratory and molecular diagnostics with the highest precision and process reliability: GMP-compliant and certified according to DIN EN ISO 13485. Production takes place under fully automated cleanroom conditions in accordance with DIN EN ISO Class 7 / GMP Standard C. Whether PCR plates for in vitro diagnostics (IVD), spin columns for nucleic acid purification, or components for automated sample preparation—our solutions include hygiene, complete documentation, and reproducible quality for human and veterinary diagnostics.

 

PCR and Filter plates

for IVD applications

Consumables

for molecular diagnostics & laboratory automation

Reagentbox

for secure sample storage and molecular analysis

Lab vessels

with and without lid for nucleic acid purification

Rack

stable holders for centrifuge columns

Spin Column

precisely manufactured columns for DNA/RNA isolation

Microtiter Plate

high-quality plates for reliable test series in the laboratory

 

 

 

 

REACTION VESSELS WITH AT LEAST 90% PCR CONTENT.

Scientific laboratories generate large amounts of plastic waste from single-use products. Yet even in this highly sensitive field, where sterility and hygiene are paramount, greater sustainability is possible. QIAGEN N.V. demonstrates this with its eco-friendly QIAwave extraction kits, which contain up to 63 percent less plastic. Among other things, reaction vessels made from post-consumer recycled (PCR) materials contribute to this. 

Case Study
FAMAC Reaction Vessel made from PCR and virgin material

Our Added Value,
Your Benefits.

STEFFEN PREUSCHOFF

SALES
LAB & DIAGNOSTICS

Benefits

Your BENEFIT: Everything from a single source.

  • Custom Development: Primary and secondary packaging tailored to your requirements.

  • Contract Manufacturing: Injection molding, packaging, and assembly—all from a single source.

  • Fully automated cleanroom production: in accordance with DIN EN ISO Class 7 / GMP Standard C.

  • GMP-compliant documentation: certified according to DIN EN ISO 13485.

  • In-house tooling: maximum flexibility and quick turnaround times.

  • Everything from a single source: from concept to series production.

 

We would be glad to discuss our advantages in a personal meeting.

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