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The RigidSafetybag from Daklapack Group integrates three packaging elements into a single unit: a 100% leak and tamper-proof Safetybag, a rigid blister-style tube holder, and sufficient absorbent material to contain any leakage from the primary receptacle. The system carries full UN3373 labelling for biological substance Category B transport, with usage instructions printed directly on the packaging. The destructive seal and tamper-evident text in the side seals provide complete tamper evidence once applied.
The internal rigid component maintains structural integrity during transit, eliminating the need for additional cushioning or secondary containment in most shipping scenarios. The absorbent material is sized to fully capture leaked content from the primary tube or vessel, meeting standard requirements for secondary packaging in diagnostic specimen transport. The blister holder accommodates common tube diameters used in clinical and laboratory settings, with the surrounding absorbent layer typically composed of super-absorbent polymer or cellulose-based material standard for biological containment. The outer envelope or box into which the sealed RigidSafetybag is placed must itself meet UN3373 marking requirements for complete compliance.
This packaging system serves clinical laboratories, diagnostic centres, biobanks, and healthcare facilities shipping blood tubes, swabs, and other Category B biological specimens. Buyers include procurement managers for hospital networks, private diagnostic chains, and specialist logistics firms handling medical consignments. The integrated design reduces packing time and material waste compared to assembling separate absorbent pouches, rigid holders, and leak-proof bags. For trade terms, volume commitments, and lead times, buyers should contact Daklapack Group directly at their Lelystad, Flevoland facility.
| Regulatory Classification | UN3373 Biological Substance, Category B |
| Leak Proof Rating | 100% leak proof (supplier stated) |
| Tamper Evidence | Destructive seal with printed tamper text in side seals |
| Internal Construction | Rigid blister-style tube holder with surrounding absorbent material |
| Absorbent Capacity | Sufficient to fully absorb content of primary receptacle (supplier stated) |
| Primary Tube Accommodation | Standard clinical tube diameters (typical range 13-16 mm) |
| Outer Packaging Compatibility | Fits standard UN3373 envelope or box after sealing |
| Labelling | Pre-printed usage instructions and UN3373 markings |
| Material - Outer Bag | Multi-layer plastic film, typical for medical transport (standard) |
| Absorbent Material Type | Super-absorbent polymer or cellulose composite (typical for biological containment) |
Daklapack Group operates from Kamerlingh Onneslaan 6 in Lelystad, Flevoland, Netherlands, within the country's logistics corridor with access to major European distribution networks. The company's trust tier is classified as harbour, and its response rate is recorded at 0.00% with zero average response hours, indicating no active engagement data is available from the listing. The supplier's address places it in a developed industrial zone with established freight connections to Amsterdam Schiphol Airport and the Port of Rotterdam.
The listing presents Daklapack Group's patented RigidSafetybag as its featured product, with no additional company history, employee count, revenue figures, or client references provided. The supplier does not list specific certifications, ISO accreditations, or quality management systems on this product page. Buyers should verify the company's manufacturing capabilities, whether production occurs at the Lelystad address or through contracted facilities, and request documentation of UN3373 testing compliance directly from the supplier before committing to volume orders.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | <4h |
| Response Rate | New Supplier |
Before placing an order with Daklapack Group, buyers should request the UN3373 test report and certificate of compliance from an accredited testing laboratory, verifying that the specific lot or production batch meets current transport regulations. Confirm the exact tube capacity range, absorbent volume rating in millilitres, and whether the product has undergone IATA air transport validation. Ask for material safety data sheets for all components, particularly if your facility requires disclosure of chemical constituents for occupational health compliance. Given the zero response rate recorded, establish direct contact through multiple channels, email and phone, to gauge current operational status before relying on this supplier for critical specimen transport needs.
For logistics and shipping, confirm with Daklapack Group whether deliveries originate from the Lelystad address or a separate distribution centre, as this affects lead time calculations and Incoterms selection. Typical Incoterms for Netherlands-origin medical packaging are EXW, FCA, or DAP depending on buyer preference and courier arrangement. Payment terms should be negotiated directly, common structures for first orders being 30% deposit with balance against shipping documents, or full prepayment for small trial orders. Request the estimated production lead time in working days, whether stock is held or made-to-order, and the minimum order quantity for both standard and customised configurations. Courier options through Amsterdam Schiphol or road freight via Rotterdam should be discussed based on destination and urgency.
Quality assurance for biological specimen packaging requires incoming inspection of sample lots before full commitment. Buyers should conduct seal integrity testing on arrival, using dye penetration or pressure decay methods appropriate to the claimed 100% leak-proof rating. Verify that UN3373 markings are legible, correctly positioned, and include the proper shipping name and hazard identification. Document any variation in absorbent material quantity or distribution within the bag cavity. For ongoing supply, request batch test records and supplier audit access if your quality management system requires second-party assessment. Retain certificates of conformance and test reports for regulatory inspection, as transport of non-compliant biological materials carries significant liability for the shipper.
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Securing a reliable supply chain for 3 In 1 Secondary Leak Proof Packaging is critical for maintaining your business operations. Daklapack Group, a verified supplier located in Netherlands, provides high-quality 3 In 1 Secondary Leak Pro ready for international export. By connecting directly with this supplier, buyers can bypass intermediaries, negotiate custom wholesale pricing, and arrange bulk shipments. This product is a key offering within the Packaging Bags industry, catering to distributors, wholesalers, and importers worldwide.
Navigating the complexities of global sourcing is easier when you have direct access to the right manufacturers and exporters. When importing 3 In 1 Secondary Leak Pro from Netherlands, buyers can discuss shipping logistics, packaging requirements, and preferred payment terms directly with Daklapack Group. This seamless communication is powered by EximNext, a premier global B2B marketplace that connects ambitious buyers with verified global sellers across every major industry.
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When importing 3 In 1 Secondary Leak Pro from Netherlands, buyers should consider shipping terms (FOB, CIF, EXW), customs documentation requirements, and payment security. Contact the supplier to discuss the best logistics options for your destination country.
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