CIM AUX + C/HRM

Catalogue number CIM AUX + C/HRM, listed by Medical Measurement Systems B.V., Netherlands, under System, Gastrointestinal Motility (Electrical). 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
5510(k) clearances naming this product code

Who Else Makes It

Registered in Shanghai. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FFX
Manufacturer City Province Registered as Device types
Ankon Medical Technologies (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 2

Record

Regulatory record for CIM AUX + C/HRM
Listed by Medical Measurement Systems B.V., Netherlands
FDA product code FFX
Device type System, Gastrointestinal Motility (Electrical)
Device class Class 2
Regulation 21 CFR 876.1725
Establishment Exporter
Premarket notification Exempt
Record published 2016-09-23
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Latex Labelled latex-free
Label carries serial number

Catalogue Numbers

Catalogue numbers for CIM AUX + C/HRM
Catalogue number Size Status
CIM AUX + C/HRM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Mui Scientific H&A Mui Enterprises, Inc. 771
UniTip High Resolution Catheter Unisensor AG 183
UniTip Catheter Unisensor AG 100
ManoScan Given Imaging Ltd. 60
Diversatek Healthcare Diversatek Healthcare Inc 27
inSIGHT Ultima Diversatek Healthcare Inc 19
Endoflip Covidien LP 17
Sitzmarks Radiopaque Markers Konsyl Pharmaceuticals, Inc. 14
Zvu® Diversatek Healthcare Inc 11
Distender II Barostat G & J Electronics, Inc. 9
PriZm Diversatek Healthcare Inc 8
ManoView Given Imaging Ltd. 6

Showing 12 of 107. All products under System, Gastrointestinal Motility (Electrical)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121014 2012-08-01
K071094 2007-08-13
K060166 2006-04-21
K052338 2005-12-15
K031084 2004-03-19

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