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This offering from Discount Medical Surplus comprises expired Mini One brand balloon button low profile feeding devices in two French sizes and shaft lengths configurations. The lot contains seven units of reference M1-5-1235 (12 French x 3.5 cm) with June 2013 expiration, and two units of reference M1-5-1810 (18 French x 1.0 cm) with May 2013 expiration. All items remain in original factory packaging, unopened, though sterility has expired. These are enteral feeding access devices with low-profile internal retention balloons, designed for percutaneous endoscopic gastrostomy (PEG) maintenance or replacement.
The Mini One product line by Halyard Health (formerly Kimberly-Clark) utilises silicone or polyurethane construction for the shaft with an internal inflatable balloon for gastric retention. The 12 French diameter equates to approximately 4.0 mm outer diameter, while 18 French equals approximately 6.0 mm. Shaft length of 3.5 cm versus 1.0 cm indicates different stoma tract measurements, with shorter lengths typically for pediatric or thin-abdominal-wall patients. French sizing convention in enteral devices follows the Charriere scale where 1 Fr equals 0.333 mm. The balloon volume for retention is typically 3-5 mL sterile water for Mini One low-profile devices, though exact specifications for these specific references should be confirmed against manufacturer datasheets.
These devices are sold explicitly for non-human use: training, simulation, or veterinary applications only. The supplier requires purchaser authorisation verification for FDA-regulated items, though these expired lots fall outside current device distribution for clinical human use. Buyers should confirm their intended application complies with local regulations, as import restrictions on expired medical devices vary by jurisdiction. The supplier's address in Orlando, Florida suggests US domestic shipping advantage, though international buyers must verify customs classification and any import licensing for used or expired medical goods in their destination country.
| Product References | M1-5-1235 (7 units), M1-5-1810 (2 units) - Mini One brand by Halyard Health |
| French Size / Outer Diameter | 12 Fr (4.0 mm) and 18 Fr (6.0 mm) per Charriere scale |
| Shaft Length | 3.5 cm (M1-5-1235) and 1.0 cm (M1-5-1810) - measured from external bolster to balloon proximal edge |
| Balloon Retention Volume | Typical: 3-5 mL sterile water (exact fill volume and pressure rating to confirm from manufacturer literature) |
| Material Construction | Silicone or polyurethane shaft with silicone balloon (standard for Mini One low-profile series; exact material specification per reference to confirm) |
| Sterility Status | Expired sterility (May 2013 and June 2013); sold non-sterile, for training or veterinary use only |
| Packaging Condition | Original factory packaging, unopened |
| Regulatory Classification | FDA Class II medical device (expired; not for human implantation or therapeutic use) |
| Intended Use Restriction | Non-sterile; training, simulation, or veterinary purposes only; not for human consumption or implantation |
| Lot Quantity | 9 units total (7 + 2 mixed references) |
Discount Medical Surplus operates from 5036 Dr. Phillips Boulevard, Suite 284, Orlando, Florida 32819, United States. The supplier is classified as imported tier with harbor trust level, showing a zero percent response rate and zero recorded average response hours on the platform. No information is provided about year of establishment, inventory specialisation breadth, quality management certification, or named institutional clients. The supplier's handling of expired medical devices suggests surplus or secondary market focus rather than manufacturer-authorised distribution.
The listing carries extensive disclaimer language regarding FDA regulation, purchaser authorisation, and liability waiver. Buyers should note that the supplier explicitly disclaims certification for any specific use and requires indemnification against regulatory claims. This indicates a risk-averse legal posture typical of surplus dealers handling expired or near-expiry medical goods. No verification of cold chain history, storage conditions, or manufacturer lot traceability is provided. Prospective buyers should request inventory source documentation and confirm that the supplier holds appropriate wholesale drug or device licences in Florida.
| 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 purchasing from Discount Medical Surplus, verify that your organisation is authorised to acquire expired medical devices under applicable FDA, state, or foreign regulations. Confirm that the intended use, training or veterinary, is permissible with non-sterile expired devices in your jurisdiction. Request copies of the supplier's wholesale device licence, FDA establishment identifier if applicable, and evidence of proper storage conditions. Validate that your institution's risk management and legal counsel accept the liability waiver terms, as the supplier explicitly disclaims responsibility for any use.
For logistics, confirm whether the supplier ships from their Orlando address or uses a third-party fulfilment centre. Domestic US buyers should verify shipping carrier, cost, and whether hazardous materials classification applies to residual ethylene oxide sterilised packaging. International buyers must determine customs HS classification for expired medical devices, typically 9018.90 or 9023.00 depending on destination country interpretation, and whether import licences for used or expired medical goods are required. Insurance for shipment should cover declared value, as expired goods may have limited carrier liability. Payment terms should be confirmed, including whether credit card, wire transfer, or purchase order is accepted, and whether educational institutions receive different terms.
Upon receipt, inspect each unit for packaging integrity, confirming no punctures, moisture ingress, or UV damage that could compromise the device for training purposes. Verify reference numbers match the order, and cross-check against manufacturer datasheets for dimensional accuracy. For training use, conduct initial insertion simulation to assess material pliability and balloon inflation integrity. Document any device failure modes, balloon leakage, or shaft kinking. Maintain lot records for traceability. If re-sterilisation is attempted, validate the method against material compatibility data and log sterilisation parameters for training quality assurance. Retain packaging and IFU for curriculum documentation even if expired.
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