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4-Slot Absorbent Inserts for Clinical Specimen Transport Bags
Product Description
The absorbent pad within the clinical specimen transport bag is engineered to contain any potential leakage from specimen tubes. When used in conjunction with the transport bag, it ensures the secure and compliant transportation of biological specimens, meeting standards such as UN3373 for biohazard transport.
Dimensions:
Outer Bag: 180mm x 250mm
Absorbent Sleeve (4-slotted): 160mm x 240mm
Individual Slot Size: 40mm x 150mm (Accommodates standard specimen tubes up to 25mm in diameter)
Features
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Absorbent Material: Medical-grade cellulose nonwoven
Sterilization: EO sterilized (SAL=10⁻⁶, batch traceable)
Chemical Compatibility: Resistant to water, 75% alcohol, pH 4-9 buffers (USP Class VI)
Hazard-Free: Fluorescent-free, phthalate-free (EU REACH)
Product Information
| Feature | Description |
| Compliance | PI650 & UN3373 Certified |
| Pressure Rating | 95kPa Certified |
| Material | Durable, high-clarity PP/PE film |
| Sealing | Tamper-evident adhesive or zip-lock) |
| Absorbency | Multi-slotted absorbent sleeve for spills |
| Markings | International biohazard symbols |
Application
Hospitals and clinics
Diagnostic and research laboratories
Pharmaceutical and biotechnology companies
Transportation of infectious substances, diagnostic specimens, and other biological materials.
Company profile
- Advance International Corp is a global leader in biomedical specimen packaging, dedicated to safeguarding the integrity, safety, and compliance of clinical samples throughout the transportation and storage lifecycle.
Our Portfolio: Beyond Absorbent Sleeves
We offer a comprehensive range of specimen packaging solutions, including:
- ● UN3373/IATA-compliant specimen transport bags (with tamper-evident seals).
- ● Sterile specimen collection kits (tubes, swabs, containers).
- ● Temperature-controlled packaging (for cold chain logistics).
- ● Custom labeling and barcoding systems (for traceability).
- ● Quality & Compliance Our Core.
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We adhere to the world's strictest standards:
Certifications: FDA-registered, CE-marked, ISO 13485 (medical device quality management).
Testing: In-house labs validate fluid absorption, biocompatibility, and barrier performance.
Regulatory Alignment: Fully compliant with UN3373, IATA DGR, and OSHA 1910.1030 for biohazard transport. -
AIC collaborate with laboratories, hospitals, and biotech firms to design tailored solutions—from standard products to bespoke packaging for unique sample types (e.g., infectious materials, frozen specimens). Our R&D team prioritizes user-friendly design, cost efficiency, and adaptive technology to meet evolving industry needs.
With decades of expertise, our supply chain ensures fast delivery across 50+ countries. From off-the-shelf orders to large-scale custom projects, we provide end-to-end support—including regulatory guidance and post-sales technical assistance.











