Guangzhou King Yon Medical Tech Co ., Ltd
surgical gowns, FFP2 face mask, protective coverall, surgical suits,
Contact - Guangzhou King Yon Medical Tech Co ., Ltd
No.718, Blv San Yuan Li, Bai Yuan District,
Guang dong,guang zhou 510403
China
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Legal information - Guangzhou King Yon Medical Tech Co ., Ltd
Nature | Secondary establishment : Branch - Distribution Center - Sales Office |
---|---|
Year established | 2013 |
Describe your Company and attract Business opportunities | |
Corporate capital | 3,000,000 RMB |
Co.Registration No | 914401110701730113 |
VAT no |
914401110701730113 |
No employees | 20-49 Employees |
Kompass ID? | CN231133 |
Kompass member for | New |
Membership | Booster International |
Presentation - Guangzhou King Yon Medical Tech Co ., Ltd
We have 3 manufacturing sectors:
1) Sterile Surgical Suit with FDA 510K & TUV CE
Certificate:
Surgical Gown FDA Registration Record
Test Report Based on EN 13795-1:2019
Level 2 Test Report Based on AAMI PB70:2012
Level 3 Test Report Based on AAMI PB70:2012
Level 4 Test Report from TUV, Based on AAMI PB70:2012
2)Chinese licensed manufacturer of disposable surgical protective coverall suits to clients that include hospital groups, private clinics, retail pharmacies, and licensed wholesalers throughout the world. All our products are in compliance with CE:EN14126 (TYPE4) / SGS AAMI Level4 and China GTT Standard.
Non-medical disposable one-piece isolation gown
4)Approved protective face mask series: FFP2 NR, KN95, Surgical flat face mask and etc.
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GAGeeG (Producer, Distributor / Exporter)
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Mr. Zhixiang Deng
Deputy Manager (G.Manager)
Spoken languages English, Chinese
Mr. Weiji Zhang
Director
Spoken languages English, Chinese
News - Guangzhou King Yon Medical Tech Co ., Ltd
Surgical Suits ManufacturerEN13795 Level 3/4 FDA 510K & TUV CE
Date: 2 August, 2020 4:00 PM
End: 20 August, 2021 3:59 PM
Certificate:
Level 4 Test Report from TUV, Based on AAMI PB70:2012
Level 3 Test Report Based on AAMI PB70:2012
Level 2 Test Report Based on AAMI PB70:2012
Test Report Based on EN 13795-1:2019
Surgical Gown FDA Registration Record
We herewith declare that the above mentioned products meet the transposition into national law, the provisions of the following EC Council directives and Standards. All supporting documentations are retained under the premises of the manufacturer.
General applicable directives:
Medical Device Directive: COUNCIL DIRECTIVE 93/42/EEC
Standard Applied:
EN ISO 15223-1:2016 EN1041:2008 EN ISO 13485:2016
EN ISO 14971:2012 EN 13795:2011
Notified Body:TüV SüD Products Service GmbH, Ridlestr. 65, 80339, Munchen, Germany
Identification Number:0123
(EC) Certificate(S):G2S 073966 0008 Rev.01
Expire Date of the Certificate:2024-05-26
Start of CE Marking:2010-11-26
Place,Date of Issue:Xuchang, 2019-10-15
Surgical Suit FDA 510K & TUV CE Level 3/4 AAMI PB70
Date: 2 August, 2020 4:00 PM
Surgical Gown FDA Registration Record
Test Report Based on EN 13795-1:2019
Level 2 Test Report Based on AAMI PB70:2012
Level 3 Test Report Based on AAMI PB70:2012
Level 4 Test Report from TUV, Based on AAMI PB70:2012
ISO 13485 by TUV
We herewith declare that the above mentioned products meet the transposition into national law, the provisions of the following EC Council directives and Standards. All supporting documentations are retained under the premises of the manufacturer.
General applicable directives:
Medical Device Directive: COUNCIL DIRECTIVE 93/42/EEC
Standard Applied:
EN ISO 15223-1:2016 EN1041:2008 EN ISO 13485:2016
EN ISO 14971:2012 EN 13795:2011
Notified Body:TüV SüD Products Service GmbH, Ridlestr. 65, 80339, Munchen, Germany
Identification Number:0123
(EC) Certificate(S):G2S 073966 0008 Rev.01
Expire Date of the Certificate:2024-05-26
Start of CE Marking:2010-11-26
Place,Date of Issue:Xuchang, 2019-10-15