Watch-PAT 200i

Watch-PAT200 Device (Recertified)

Registry build 21.09.26
3manufacturers in China registered for this device type
4catalogue numbers in this listing
15510(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 Watch-PAT 200i
Listed by Itamar Medical, Israel
FDA product code MNR
Device type Ventilatory Effort Recorder
Device class Class 2
Regulation 21 CFR 868.2375
Establishment Manufacturer
Record published 2016-11-20
Record revised 2023-10-17 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment humidity 10 to 93 % RH; Storage environment atmospheric pressure 68.95 to 103.42 KiloPascal; Handling environment temperature 0 to 40 °C; Handling environment atmospheric pressure 68.95 to 103.42 KiloPascal; Storage environment humidity 0 to 93 % RH; Storage environment temperature -20 to 40 °C
Packaging Carton
Distribution end date 2023-10-15

Catalogue Numbers

Catalogue numbers for Watch-PAT 200i
Catalogue number Size Status
Watch-PAT 200i Withdrawn
Watch-PAT 200i Withdrawn
Watch-PAT 200i Withdrawn
Watch-PAT 200i Withdrawn

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
K254042 2026-07-31
K250460 2025-09-05
K223675 2023-01-06
K222331 2022-09-14
K203839 2022-03-21
K183559 2019-06-05
K180775 2018-08-17
K161579 2017-02-24
K153070 2016-07-26
K133859 2014-05-30
K102567 2011-06-02
K081982 2008-08-14
K081037 2008-06-09
K080427 2008-05-23
K042916 2004-12-29

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