About PolarSeal Tapes & Conversions Ltd
PolarSeal is solely focused on medical device contract manufacturing and healthcare material conversion. Operating within our ISO7 cleanroom facilities with ISO13485 accreditations and being FDA Regulated and Audited, PolarSeal can engineer the perfect adhesive solution.
Our extensive and ever-expanding capabilities allows us to assist global medical device companies in the manufacturing of advanced wound care, ostomy components, wearable device technology, consumer healthcare and so much more.
We understand the growing demand for skin-friendly adhesives and consumer products, and that is why we continuously invest in modern technology and advanced processes to deliver fully qualified products at high speeds and to the ultimate quality standards.
As a TRUSTED ADVISOR and specialists in the contract medical device manufacturing sector, PolarSeal has in-depth knowledge in combining materials and components to complex and innovative medical devices.
To lead the way in flexible material converting by solving and serving the challenges and needs of our customers globally.
To consistently provide the highest levels of quality and support, by an in-depth understanding of the needs of our customers, and the ways in which we will provide solutions to these needs.
As part of the national and international job creation efforts, PolarSeal strives to continuously provide new opportunities. Alongside new roles enabled by company growth, PolarSeal onboards ‘KickStarter’ schemes developed by the Government to assist in the prevention of unemployment and provide futures for the next generation.
Our equal opportunities mission drives us to ensure that we can empower as many individuals as we can through job creation, knowledge transfer, enrichment, and wellness.
Original registration to BSEN/ISO 9001 Standard
First Class 10,000 Cleanroom brought on stream
Certification to ISO13485:2003 Medical Device Standard
2nd ISO7 Cleanroom (Class 10,000) brought on stream
3rd ISO7 Cleanroom (Class10,000) brought on stream
7th Servo Converting machine ordered
Acquisition of a new 36,000ft2 production facility in Suffolk
Registration with FDA
Certification to d. MDD 93/42/EEC
Patent awarded for woundcare product and manufacturing process
30th Production line validated
4,000 square foot clean production area
4th 2,000 square foot cleanroom installed
Thermoforming & flow wrapping packing process added in addition to in-line pouch lines