Personal Protective Equipment Available
| PRODUCT NAME | DESCRIPTION | SPECIFICATION NUMBER | STANDARDS TESTED AGAINST | Enquire |
|---|---|---|---|---|
| Face mask | FFP2 (DTCX3) | IPG/005 | EU Directives 89/686/EEC EB149:2001+A1:2009 | Enquire |
| Face Mask | N95 (DTCX3) | IPG/005a | FDA Approved NIOSH Approved | Enquire |
| Face Mask | N95 SQ100CVb | IPG/010 | FDA Approved NIOSH Approved | Enquire |
| Face Mask | KN95 / FFP2 | IPG/012 | Approved German Authority Technical Efficiency EU 2020/403 13/03/20 on conformity assessments and market surveillance procedure in the context of the COVID-19 risk EN 149:2001+A1:2009 EN1374-7:2008 | Enquire |
| Face Shield | Face Shield (PET) | IPG/006 | Medical Device Directives Class 1 ISO EN 1497:2012 ISO EN 15223-1:2016 EN 1041:2013 EN 166:2001 | Enquire |
| Gown | Non-Surgical | IPG/007 | Medical Device Directives 93/42/EEC Class 1 | Enquire |
| Nitrile Gloves | Type C, Nitrile Gloves | IPG/001 | 374-1:2003, EN372-2:2003 EN374-3:2003 EN42:2003 +A1.2009 EN374-2:2014 EN16523-1:2015: EN374-4:2013 | Enquire |
| Nitrile Gloves | Type C, Nitrile Gloves | IPG/002 | EN374-1:2003 EN420:2003+A1:2009 EN455-1:2000 EN455-2:2015 EN455-3:2015 Clause 4.4 &4.6 Annex II of PPE Regs 2016/425 cat III | Enquire |
| Surgical Face Mask | Non-Woven 3 ply Type IIR (Blue) | IPG/004/4a | Medical Device Directives 93/42/EEC Annex V EN 14683:2014 Annex B FDA Approved | Enquire |
| Surgical Face Mask | Non-Woven 3 ply Type IIR | IPG/008 | EN 14683:2019 + AC:2019(E) Annex B EN14683:2019 +AC:2019(E) Annex C EN 14683:2019+AC:2019(E) Annex D ISO 22609:2004 | Enquire |
| Surgical Face Mask | Non-Woven 3 ply Type IIR | IPG/011 | Medical Device directives 93/42/EEC Class 1 Annex VII EN ISO 13485:2016 EN 14683:2019+AC:2019(E) Annex B, Annex C & Annex D ISO 22609:2004 | Enquire |
| Sanitiser | Hand Sanitiser 75% Alcohol 100ml | IPG/013 | WHO Regulated Formula Approved in UK by way of Critical Situation Permit | Enquire |
| Sampling Swabs | Sterile Disposable Sampling Swabs | IPG/014 | Medical Device Directive 93/42/EEC Annex V IVD MD Directive 98/79/EC NOT Annext II and NOT self test EN ISO 15223-1:2012 EN 1041:2008 EN ISO 14971:2009 Module A Gamma Sterilisation | Enquire |
| COVID 19 Antibody Test Kit | Antibody Testing Kit | IPG/003 MD420 | In vitro diagnostics Medical Device Directives 98/79/EC EN ISO 13485:2016 | Enquire |
| COVID 19 Antibody Test Kit | 2019-Novel Coronavirus (2019-nCoV) IgG / IgM Detection Kit (Colloidal Gold- Based) | IPG/015 MD422 | Invitro Medical Device Directive 98/79/EC Annex III EN ISO 13485:2016, EN ISO 1497:2012, EN 13975:2003, EN ISO 18113-2:2011, EN ISO 18113-4:2011, EN 13612:2002/AC:2002, EN ISO 17511:2003, EN ISO 15193:2009, EN ISO 15194:200+, EN ISO 23640:2015, EN 13641:2002, EN 1041:2008, ISO 15223-1:2016 | Enquire |
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Get your copy below and contact us for info and pricing.
Note: You must ensure a product meets your specific requirements and that you have the appropriate approvals to import and/or sell in your country. IPG cannot be held liable if you are unable to import and use/sell them in your country.
IPG provides bulk supplies of all its items worldwide, we do not hold stock (unless stated otherwise) and all transactions are on an order to supply basis.