About Lina Consulting Ltd. Sti. - Medical Clothing Supplier in Turkey

Lina Consulting Ltd. Sti. operates from Turkey and currently lists five distinct medical products in its catalogue. The supplier’s portfolio includes items that fall under categories such as medical clothing, medical gloves, medical equipment and machinery, medical face masks, medical thermometers, disposable face masks, infrared thermometers and diagnostic kits. Among the active listings are swabs, goggles, sanitizer gel, a 5‑ply KN95 mask and an N95 mask. Each product is identified with an HS‑code where applicable, linking the items to the relevant customs tariff headings. The catalogue reflects a focus on consumables and protective equipment used in healthcare settings.

The swab entry is recorded under HS code 9018.39 and is described as having a nylon flocked fiber tip or a medical‑grade cotton tip, depending on the product line. The goggles entry does not include an HS code but is classified as protective eye‑wear for medical use. The sanitizer gel is listed without an HS code and is positioned as a hand‑disinfection solution. Both mask variants - a 5‑ply KN95 mask and an N95 mask - share HS code 6307.90 and are made from non‑woven polypropylene, with the KN95 employing spunbond plus meltblown layers and the N95 using meltblown filter media. These specifications align with standard protective‑equipment classifications used in international trade.

Product Range and Specialties of Lina Consulting Ltd. Sti.

The catalogue’s swabs correspond to specimen‑collection devices that are commonly produced with either nylon flocked tips for rapid sample release or cotton tips for traditional applications. In the medical market such swabs are typically supplied sterile, comply with ISO 13485 manufacturing requirements and are tested for tip integrity and absorption capacity, often expressed in microlitres (µL).

Goggles listed without an HS code are usually made of polycarbonate or acetate frames with anti‑fog coatings and must meet standards such as EN 166 or ANSI Z87.1 for impact resistance and optical clarity. Sanitizer gels are generally formulated with ethanol or isopropanol concentrations between 60 % and 80 % v/v, following WHO or FDA guidelines for hand‑disinfection efficacy. The 5‑ply KN95 and N95 masks fall under the non‑woven polypropylene family; KN95 masks are required to achieve ≥95 % filtration efficiency for particles of 0.3 µm under the Chinese GB 2626‑2006 standard, while N95 masks meet the US NIOSH 42CFR Part 84 criteria for the same efficiency level. Both mask types are often graded by breathability (ΔP) and fluid resistance (ASTM F2100).

Trade and Export Information - Lina Consulting Ltd. Sti.

Turkey is a recognized exporter of medical consumables and protective equipment, with established trade routes to the European Union, the Middle East and North America. Products classified under HS 9018.39 (swabs) and HS 6307.90 (protective masks) are subject to customs documentation that typically includes a commercial invoice, packing list, certificate of origin and, where required, a CE Declaration of Conformity or FDA 510(k) clearance. Buyers frequently request test reports such as bacterial filtration efficiency (BFE), particle filtration efficiency (PFE), and flammability ratings for masks, as well as sterility certificates for swabs and goggles. Standard packaging for these items includes sealed polyethylene bags for individual masks, bulk cartons for swabs, and cardboard boxes with inner cushioning for goggles and sanitizer gel. Common Incoterms used in Turkish medical‑goods exports are FOB Istanbul, CIF Mediterranean ports, or DAP to the buyer’s destination, with temperature‑controlled containers employed for sanitizer gel shipments.

Typical importers of Turkish medical protective gear are hospitals, distributors of personal protective equipment (PPE), and government procurement agencies. Regulatory scrutiny often involves conformity to EU MDR for medical devices, US FDA regulations for N95 respirators, and local health authority approvals. Exporters must ensure that the non‑woven polypropylene used in masks complies with REACH restrictions on hazardous substances and that any biocidal claims for sanitizer gel are backed by appropriate efficacy data.

Sourcing from Lina Consulting Ltd. Sti. - Buyer Guidance

When sourcing from Lina Consulting Ltd. Sti., buyers should request the latest ISO 13485 certificate, CE Declaration of Conformity for masks, and any FDA clearance documents for N95 respirators. Sample swabs should be delivered sterile and accompanied by a sterility test report; mask samples should include filtration efficiency and breathability test results. Verify that the material safety data sheet (MSDS) for the sanitizer gel specifies the alcohol concentration and any preservatives used, and confirm that the packaging meets the buyer’s shelf‑life requirements.

Before placing a purchase order, confirm the minimum order quantity (MOQ) for each product line, typical lead times (often 4‑6 weeks for masks and 2‑3 weeks for swabs and goggles), and the agreed Incoterm. Request a full packing list indicating unit counts per carton, container loading plans (e.g., 20‑ft container capacity of approximately 1,200 KN95 masks) and any temperature control measures for gel shipments. Conduct a pre‑shipment inspection or arrange third‑party verification to ensure compliance with the cited standards and to reduce the risk of non‑conformity at customs.

What medical products does Lina Consulting Ltd. Sti. list in its catalogue?

The catalogue includes swabs (HS 9018.39), goggles, sanitizer gel, a 5‑ply KN95 mask and an N95 mask (both HS 6307.90). Each entry specifies the primary material, such as nylon flocked fiber or medical‑grade cotton for swabs and non‑woven polypropylene for the masks.

Which HS codes are associated with the listed masks?

Both the 5‑ply KN95 mask and the N95 mask are recorded under HS code 6307.90, which covers other made‑up textile articles, including protective face masks.

What material is used for the swab tips?

The swabs are described as having either a nylon flocked fiber tip or a medical‑grade cotton tip, depending on the product line.

Are certifications such as CE or FDA required for these products?

While the supplier’s facts do not list specific certifications, buyers typically request CE marking for masks sold in the EU and FDA 510(k) clearance for N95 respirators in the United States, as well as ISO 13485 for the overall manufacturing system.

What are typical quality tests for the masks?

Standard tests include particle filtration efficiency (≥95 % for 0.3 µm particles), breathability measured as pressure drop (ΔP), and fluid resistance according to ASTM F2100. Test reports should be provided before shipment.

What packaging format is used for the sanitizer gel?

Sanitizer gel is usually packed in sealed plastic bottles or sachets, placed in secondary cardboard boxes for bulk handling. Buyers should confirm that the packaging complies with any local labeling and safety requirements.

What is the usual lead time for the listed products?

Lead times commonly range from 2‑3 weeks for goggles and sanitizer gel to 4‑6 weeks for the KN95 and N95 masks, depending on order size and production scheduling.

How can a buyer request a sample?

A buyer can request a sample by contacting the supplier with the specific product name, indicating the desired quantity (often a single unit or a small pack), and asking for accompanying test certificates or material safety data sheets.