Moor Instruments Ltd

Non-sterile Oxygenation, and Laser Doppler combined Probes

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
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 Moor Instruments Ltd
Listed by Moor Instruments Ltd., United Kingdom
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) K112826
Record published 2016-07-08
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment atmospheric pressure 80 to 106 KiloPascal; Handling environment humidity 0 to 80 % RH; Handling environment temperature 15 to 30 °C; Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 0 to 80 % RH; Storage environment temperature 5 to 45 °C
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Moor Instruments Ltd
Catalogue number Size Status
moorVMS-OXY In distribution
NON-STERILE OXYGENATION AND LASER DOPPLER COMBINED PROBES In distribution

Same Product Code

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Product Sold by Catalogue numbers
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Showing 12 of 30. All products under Oximeter, Tissue Saturation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K112826 2012-10-10

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