SLP Thermistor LOW Cost

Catalogue number SEN600S, listed by Somnomedics AG, Germany, under Ventilatory Effort Recorder. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Fujian (1), Jiangsu (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNR
Manufacturer City Province Registered as Device types
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11

Record

Regulatory record for SLP Thermistor LOW Cost
Listed by Somnomedics AG, Germany
FDA product code MNR
Device type Ventilatory Effort Recorder
Device class Class 2
Regulation 21 CFR 868.2375
Establishment Specification developer, Manufacturer
510(k) K071556
Record published 2019-04-12
Record revised 2025-02-10 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for SLP Thermistor LOW Cost
Catalogue number Size Status
SEN600S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sleepsense S. L. P. Scientific Laboratory Products Ltd 182
TriplePlay Dymedix Diagnostics Inc 71
Embla S. L. P. Scientific Laboratory Products Ltd 36
Grass S. L. P. Scientific Laboratory Products Ltd 31
Xltek Embla Systems 30
Alice NightOne Respironics Inc. 22
Onera STS Onera B.V. 21
Natus S. L. P. Scientific Laboratory Products Ltd 21
Night Shift Advanced Brain Monitoring, Inc. 19
Neurovirtual Neurovirtual USA, Inc. 18
SOMNOtouch Resp accessory Somnomedics AG 18
zRIP Respironics Inc. 17

Showing 12 of 259. All products under Ventilatory Effort Recorder

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K140861 2015-01-30
K081485 2008-09-18
K071556 2007-07-18
K060708 2007-01-24

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