In an interventional suite the consumable is not a single item but a sequence: drape, table cover, gown, guidewire bowl, syringe, gauze, catheter-securing device, waste bag. Assembling that sequence from a stock room costs nursing time in the most expensive room in the hospital, and every separate item brings its own sterile barrier to open and its own lot number to record. A configured interventional procedure bag exists to remove that work.

This category covers the single-use interventional pack: the sterile bag or pack that carries the accessories a catheterisation, angiography or minor interventional procedure needs, configured to the procedure rather than to a generic list. Content, barrier fabric, drape size and the order in which items are presented are set with the clinician at the design stage, then reproduced identically pack after pack.

What interventional buyers assess is whether the pack matches the procedure they actually perform — an extra item nobody uses is waste on every case, and a missing item means breaking sterility to fetch it. That is why this category is quoted as a configuration, not as a catalogue number.

Assembling interventional packs by hand from ward stock? Send us the procedure and the item list you currently gather. We will propose a single sterile pack with the same content in the order your team uses it — and quote it per case so you can compare against your current consumable cost.

Disposable Interventional Surgical Bag Sterile Single Use

Interventional Consumables in practice

Diagnostic catheterisation and angiography — drape, table cover and accessory pack for the access sequence
Vascular access procedures — pack configured around sheath and guidewire handling
Minor interventional procedures — sterile field plus accessory set for short cases
Day-case and outpatient intervention — single pack per case for fast room turnover
Emergency and casualty intervention — pre-assembled pack for cases that cannot wait for assembly
Radiology and imaging suites — barrier items sized for the imaging table and C-arm

Choosing the right Interventional Consumables

Design the pack around one case, then multiply it:

Start from the procedure list, not the catalogue. Write down what is opened for a standard case in your room and in what order. That list is the pack specification — the most common mistake in pack design is adding items "in case", which every case then pays for.
Barrier fabric and drape size. Confirm the drape dimensions against your table and patient positioning, and the barrier performance your infection-control policy requires. A drape that is correct for one table can be short on another.
Presentation order. Items are sequenced in the pack so the team opens them in the order they use them. This is a small detail that decides whether the pack feels designed or dumped.
Reproducibility. The value of a procedure pack is that pack 500 is identical to pack 1. Confirm the change-control arrangement before ordering — content changes should be agreed with you, not introduced by the supplier.

Interventional Consumables specifications

Component	Typical specification	Options	Purpose
Sterile bag / outer pack	Sterile barrier, peel-open	Size per procedure	Aseptic presentation of contents
Procedure drape	SMS or film-fabric, fenestrated	Dimension per table	Sterile field, table coverage
Table cover / C-arm cover	Fitted or flat	Imaging-compatible	Barrier over equipment
Accessory set	Syringes, bowls, gauze, kidney dish	Configured to case	The working sequence
Securing and dressing items	Catheter securement, dressing	Per access type	Post-procedure fixation
Waste bag	Peel-and-stick	With or without	Contained disposal at the table

Note: the pack is quoted as a configuration. Content, sizes and sequence are agreed with your clinical team before the first production run.

How we control quality for Interventional Consumables

Interventional packs are judged on sterility assurance and on reproducibility:

Sterile barrier integrity. Packaging validated to ISO 11607 — seal strength, peel performance, and transit-drop testing so the barrier arrives intact rather than arriving "probably intact".
Sterility and SAL. EO sterilization to SAL 10⁻⁶ with the cycle recorded against the pack lot; residuals tested to ISO 10993-7 limits.
Biocompatibility. ISO 10993 testing for the patient-contacting contents and for the barrier materials used on skin.
Configuration control. The pack specification is locked and versioned; changes are notified to you rather than absorbed silently, so what your team trained on is what arrives.
Traceability. Pack lot links to the lots of the components inside it — this is what makes a recall scope-able to exactly the affected cases.
Quality system. ISO 13485 manufacturing, CE marking under EU MDR, with the technical file extracts your registration holder needs.

Common questions about Interventional Consumables

Can the procedure pack be configured to the exact case we perform?

Yes — that is the point of the category. We start from your written case list: what is opened for a standard procedure and in what order. Content, drape size, barrier fabric and presentation sequence are agreed with your clinical team, then locked as a versioned specification so every subsequent production run is identical. Items that are only occasionally needed can be left out and stocked separately.

What is the minimum order quantity for a custom interventional pack?

MOQ depends on the number of components and the level of customization: a pack built from standard items with your label carries a lower MOQ than one with custom drape dimensions or bespoke contents. As a guide, custom sterile packs are quoted at case-quantity volumes rather than unit volumes. Send the item list and your annual case count and we will confirm the MOQ for that configuration.

How is the sterile barrier validated?

Packaging is validated to ISO 11607: seal strength and peel performance, accelerated aging for shelf life, and distribution (transit) testing so the sterile barrier is proven to arrive intact after real shipping rather than assumed to. Validation reports are available for your technical file.

Do you notify us before changing the content of our pack?

Yes. Each configuration is versioned and changes require your written agreement before they are introduced. This matters more than it sounds: if a supplier silently substitutes an item, the team discovers it while a patient is on the table, and your audit trail no longer matches what was used.

Which procedures can these packs cover?

The category is built around catheterisation, angiography, vascular access and general minor interventional procedures, but the configuration mechanism is the same for any suite that assembles a sterile field from multiple items. Tell us the procedure mix and we will propose a small number of standard packs to cover most cases rather than one pack per procedure.

What documentation accompanies an interventional pack order?

Each shipment carries the pack lot number and expiry, and includes the manufacturer-side documentation: ISO 13485 certificate, CE marking certificate and technical file, declaration of conformity, sterilization reports, ISO 11607 packaging validation and biocompatibility reports. Specimen documentation can be provided before a first order.

Interventional Consumables