Injection port, flexible wings and transparent flashback chamber
Sterility & packing
Sterile; individually packed in peel-open blister packaging
Sizes listed in the catalogue
Gauge
Hub colour
Catheter length
Listed flow rate
14G
Orange
45 mm
270 ml/min
16G
Grey
45 mm
200 ml/min
17G
White
45 mm
125 ml/min
18G
Green
45 mm
90 ml/min
20G
Pink
32 mm
55 ml/min
22G
Blue
25 mm
36 ml/min
24G
Yellow
19 mm
18 ml/min
26G
Violet
19 mm
13 ml/min
Source: Healthcare catalogue · Page 9.
Catalogue options are a reference for your enquiry. Confirm the exact variant and current specification in your quotation.
BUYER TECHNICAL REVIEW
From catalogue reference to agreed specification.
Use the published catalogue details as a starting point. Complete the open requirements for your selected model and destination before an order is approved.
CATALOGUE REFERENCE
Source-backed product fields
The specification section above reproduces the supplied catalogue fields and any listed variant table. These are catalogue statements, not a supplier approval or a guarantee of current availability.
The checklist below requests evidence and commercial details. A listed request does not mean the document is held, the product is registered, or the requirement has been approved.
Gauge and catheter length; radiopaque FEP; port and wing configuration.
Request the selected model’s flow-rate specification and test basis. Match it to the gauge and length, rather than treating the catalogue rate as a guaranteed value.
Confirm catheter and needle dimensions, hub connection, protective pack and sample reference.
01Use & variant+
Intended use & instructions
Request the manufacturer’s intended-use statement and current instructions for the exact model and destination.
Model & specification revision
Record the manufacturer, manufacturing site, model code, selected variant and agreed specification revision.
Materials & declarations
Request component materials and latex, DEHP or other phthalate declarations where relevant to the selected product.
02Sterility & shelf life+
Supplied sterility status
Confirm sterile, non-sterile or ready-to-sterilize presentation. Where sterile, request the method and supporting validation or batch-document requirements.
Shelf life & storage
Request the labelled shelf life, supporting basis, storage conditions and minimum remaining shelf life required at delivery.
03Packing & shipment data+
Unit, inner box & carton
Confirm units per immediate pack, packs per inner box and units per master carton. Separate each packing level.
Carton measurements
Request outer carton length × width × height, measurement units, net weight and gross weight for the selected packing.
Origin & markings
Confirm the manufacturer and country of origin for the selected supply; request carton markings and origin-document requirements.
04Documents for your market+
Destination & importer role
Specify the destination country, intended sales channel, local importer or registration holder, and required label languages.
Standards & certificate scope
Request an applicable-standards list and product or manufacturer documents, with issuer, holder, site, covered models, validity and verification references.
Market-specific evidence
Agree which registration, conformity, test, biocompatibility or other documents are applicable and available for this product and market.
05Samples & commercial basis+
MOQ & sample policy
Request minimum quantities by variant and branding option, sample quantity, sample cost and sample-freight responsibility.
Lead time & quotation
Confirm the lead-time start event, production and transit basis, USD pricing, agreed delivery responsibilities, and advance-payment or LC terms.
Private-label approval
Confirm label claims, artwork version, languages, manufacturer details, approval owner and approved physical or digital reference.
06Inspection & change control+
Approved sample & product images
Request photographs of the selected product, packaging and markings. Record the approved sample or drawing reference; catalogue images alone are not a supply approval.
Inspection & release
Agree inspection checkpoints, acceptance criteria, responsible reviewers and shipment-release authority. Confirm any independent-inspection arrangement.
Traceability, changes & complaints
Request the lot-identification format, document handover, change-notification agreement and complaint or nonconformity escalation contacts.
WORKING DOCUMENT
Prepare a technical request
Editable CSV for your purchasing team. Keep requested values, supplier responses and evidence references in separate columns.
Request template R1 · 4 October 2026 · English · Not a certificate or approved specification
Downloading a template does not submit an enquiry. Send your completed requirements to our team so that the selected specification and evidence can be reviewed.
PRODUCT DNA
The decisions behind your product.
Use these prompts to prepare your sourcing brief. Confirm specifications and supporting evidence for the selected product.
Simplified diagram for procurement discussion. Not to scale or for clinical use.
Complete product view. Select a numbered detail to explore.
Select a detail to explore.
01Needle+
The catalogue specifies siliconized stainless steel. Confirm the exact variant and protective packaging.
02Catheter+
The catalogue specifies radiopaque FEP. Review gauge and catheter length together.
03Flashback chamber+
A transparent flashback chamber is listed. Review the selected configuration against a sample.
04Flexible wings+
Flexible wings are listed. Include this design requirement in your product brief.
05Injection port+
An injection port is listed. Confirm the port configuration on the selected variant.
06Radiopacity+
The catheter is described as radiopaque FEP. Request evidence for the selected product; the diagram does not establish the location of a separate strip.
Review the details and add your quantity before saving to your enquiry.
01Procurement checklist+
Specify gauge, catheter length, material, port configuration and quantities by size.
02Common selection mistakes+
Do not compare quotations by gauge alone. Match the complete configuration and packing.
03Packaging options+
The catalogue lists sterile individual peel-open blister packaging. Confirm inner-box and master-carton quantities.
04Private-label opportunities+
Discuss artwork, label languages, pack information and approval samples. Feasibility and minimum quantities are confirmed per product.
05Quality parameters to confirm+
Request the applicable specification, sterility information, batch identification and supporting product documents.
06Before use & handling+
Request the manufacturer-approved instructions for the exact variant, intended use, handling, storage and shelf life. Have the applicable information reviewed by a qualified professional in your market before use.
Every enquiry is personally reviewed by the founders of Khetsi International.
Preferences to confirm: cannula gauge, catheter length, injection port, wings and blister packing.
Add the required quantity and its unit, together with your destination and preferred timeline. Final specifications and packing are confirmed in the quotation.
Review the source information
The original catalogue page provides the supplied product reference. Manufacturer codes, documentation, availability and commercial terms are confirmed for the selected variant.