Mimosa

Catalogue number MIMOSA Pro, listed by Mimosa Diagnostics Inc., Canada, under Oximeter, Tissue Saturation. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (2), Sichuan (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 MUD
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13
Measurement Specialties Chengdu Chengdu Sichuan Contract manufacturer 3
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57

Record

Regulatory record for Mimosa
Listed by Mimosa Diagnostics Inc., Canada
FDA product code MUD
Device type Oximeter, Tissue Saturation
Device class Class 2
Regulation 21 CFR 870.2700
Establishment Complaint-file establishment, Manufacturer
510(k) K190334
Record published 2022-02-01

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for Mimosa
Catalogue number Size Status
MIMOSA Pro In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Invos Covidien LP 54
Nonin Nonin Medical, Inc. 30
Fore-Sight Elite® Cas Medical Systems, Inc. 12
Fore-Sight® Cas Medical Systems, Inc. 9
ForeSight Edwards Lifesciences Technology Sarl 7
Spectros T-Stat Spectros Corporation 7
Component Neuromonitoring System Moberg Research, Inc. 6
HyperView Hypermed Imaging, Inc. 6
O3 Masimo Corporation 5
Mespere Mespere Lifesciences Inc. 3
SnapshotNIR Kent Imaging Inc 2
Moor Instruments Ltd Moor Instruments Ltd. 2

Showing 12 of 30. All products under Oximeter, Tissue Saturation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190334 2019-11-01

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