Mark 5 Nuvo 10

230V Ocsi 10LPM Oxygen Concentrator -- Private Labeled FOR GCE Mediline, UK Plug

Registry build 21.09.26
22manufacturers in China registered for this device type
7catalogue numbers in this listing
7510(k) clearances naming this product code
9recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Guangdong (5), Beijing (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CAW
Manufacturer City Province Registered as Device types
Foshan Kycare Medical Equipment Co., Ltd. Foshan Guangdong Contract manufacturer 3
Jakamed Instruments Co., Ltd. Changsha Hunan Contract manufacturer 2
Jiangsu Jumao X-Care Medical Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 37
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Jiangsu Yuyue Medical Equipment & Supply Company Limited Jiangsu Jiangsu Contract manufacturer 17
Tianjin Choice Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 12
Danyang Huayi Medical Supply & Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 11
Shandong Moonlight Electronics Tech Co., Ltd. Weifang Shandong Manufacturer 11
Honsun (Nantong) Co., Ltd. Nantong Jiangsu Contract manufacturer 9
Beijing Choicemmed Technology Co., Ltd. Beijing Beijing Repacker / relabeller 9
Foshan Care Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 3
Zhengzhou Olive Electronic Technology Co., Ltd. Zhengzhou Henan Manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Generator, Oxygen, Portable

Record

Regulatory record for Mark 5 Nuvo 10
Listed by Nidek Medical Products, Inc., United States
FDA product code CAW
Device type Generator, Oxygen, Portable
Device class Class 2
Regulation 21 CFR 868.5440
Establishment Manufacturer, Exporter
510(k) K093308
Record published 2016-08-24
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number
Storage Storage environment atmospheric pressure 64 to 101 KiloPascal; Storage environment humidity 15 to 95 % RH; Storage environment temperature -20 to 60 °C

Catalogue Numbers

Catalogue numbers for Mark 5 Nuvo 10
Catalogue number Size Status
1005 In distribution
1005GC In distribution
1005GCUK In distribution
595NSH In distribution
1005NI In distribution
1005UK In distribution
595 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeVilbiss DeVilbiss Healthcare LLC. 50
EverFlo Respironics Inc. 32
Mark 5 Nuvo Lite Nidek Medical Products, Inc. 30
SimplyGo Mini Respironics Inc. 26
X-PLO2R Belluscura, LLC 17
Mark 5 Nuvo 8 Nidek Medical Products, Inc. 12
ViveBreathe Vive Health LLC 11
Invacare® HomeFill® Oxygen System Invacare GmbH 11
Discov-R Belluscura, LLC 11
NewLife Elite Caire Inc. 10
NewLife Elite Airsep Corp. 10
Rhythm Healthcare Qingdao Kingon Medical Science AND Technology Co., Ltd. 9

Showing 12 of 187. All products under Generator, Oxygen, Portable

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192693 2020-05-07
K123738 2013-02-28
K093308 2010-01-14
K082566 2008-12-03
K040892 2004-04-29
K032509 2004-03-18
K883591 1988-11-02

Recalls

9 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 7889 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 3638 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 14,585 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 1599 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 335 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 82 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 730 units 2017-03-21
2012-05-01 Class I Component design/selection Capacitor failure may result in a fire hazard and loss of supplemental oxygen. 18114 units 2017-03-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer