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The NETCELL™ PVA Nasal Pack range, provides an immediate and effective solution for controlling post-operative bleeding.
• Specifically designed for use after septal, turbinate and rhinoplasty surgery
• Provides gentle, equal pressure within the nasal cavity when absorbing post-operative bleeding
• Manufactured from ultra-smooth, biocompatible PVA sponge for improved patient comfort
• Available with Integral airway tube for improved venting and reduced risk of obstruction
• Layered slimpack option allows thickness to be customised to individual requirement
• Supplied sterile, single use only, declared 5 year shelf life

  10-095 Standard3.0 x 1.5 x 2.020
 10-100Standard 4.5 x 1.5 x 2.020
10-100T Standard with airway tube 4.5 x 1.5 x 2.020
 10-101Slimpack4.5 x 1.0 x 2.0 20
10-105 Standard 6.0 x 1.5 x 2.020
10-105T Standard with airway tube 6.0 x 1.5 x 2.020
10-106 Slimpack6.0 x 1.0 x 2.020
10-110 Standard 8.0 x 1.5 x 2.020 
10-110T Standard with airway tube 8.0 x 1.5 x 2.0 20 
10-111 Slimpack8.0 x 1.0 x 2.0 20 
10-111T Slimpack with airway tube8.0 x 1.0 x 2.0 20 
10-115Standard 10.0 x 1.5 x 2.020 
10-116Slimpack10.0 x 1.0 x 2.020 

Nasal Pack 100% Polyvinyl Alcohol Sponge (PVA)
Retrieval String Braded Spring Polyester – Medical – Dacron ® Polyester Fibre
Silicone Tubing 100% Silicone Platinum Cure
Pouch Packaging Tyvek/Film 

PVA sponge ENT products are designed to staunch blood loss after invasive surgery or traumatic injury in ENT surgery. The
PVA sponge reacts quickly to absorb blood and body fluids. PVA is biocompatible and in some instances can be used for postoperative
tissue support and to carry medication to the operative site (where specified in the Instructions for Use).
Nasal Packs are intended for use after septal, Turbinate and Rhinoplasty surgery and provide gentle equal pressure within the
nasal cavity when absorbing post-operative bleeding. Patient comfort can be enhanced by using an airway tube. The
slimpack version nasal pack has been developed for use in conjunction with a nasal splint following septal surgery.

Products are sterilised by Gamma irradiation from a Cobalt 60 source in accordance with a validated 25 kGy cycle. Sterilisation is carried out in accordance with the requirements of ISO 11137:2013 and the 25 kGy dose is substantiated by VD25 Method Max testing.

The instructions for use and suggested surgical technique are supplied in the form of a multi-lingual leaflet with instructions given in diagram form where appropriate. The international symbols used on the packaging are explained in each language. A leaflet is supplied with each product.

The range of PVA sponge products is supplied sterile and intended for short-term use in the nasal cavity. Therefore classification is Class I Sterile, (rule 5, Annex IX, 93/42/EEC Medical Devices Directive).