Radmedix AcuitySDR+

Radmedix AcuitySDR+: 2 catalogue numbers listed by RadmediX, LLC, United States, under System, X-Ray, Stationary. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (3), Beijing (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code KPR
Manufacturer City Province Registered as Device types
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shanghai, Medical Equipment Ltd. Shanghai Shanghai Contract manufacturer 10
Carestream Health, Inc., Global R&D Center Shanghai Shanghai Specification developer 8
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Orich Medical Equipment (Tianjin) Co., Ltd. Tianjin Tianjin Manufacturer 5

Record

Regulatory record for Radmedix AcuitySDR+
Listed by RadmediX, LLC, United States
FDA product code KPR
Device type System, X-Ray, Stationary
Device class Class 2
Regulation 21 CFR 892.1680
Establishment Repacker / relabeller, Manufacturer
510(k) K193360
Record published 2020-09-18

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Liquid Chemical
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Radmedix AcuitySDR+
Catalogue number Size Status
1 In distribution
1 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Drgem Drgem Corporation 171
Q-RAD System Carestream Health, Inc. 159
DRX – Ascend System Carestream Health, Inc. 121
FDR Clinica Drgem Corporation 41
RADspeed Pro Shimadzu Corp. 31
FDR Visionary Suite Shimadzu Corp. 17
Exsys DEXi Drtech Corporation 15
Del Medical, Inc. DEL Medical, Inc. 15
GXR-Es,ecs Diagnostic X-ray System Drgem Corporation 14
X-CEL X-RAY Corporation Arquilla, Inc. 14
DRX-Evolution Plus System Carestream Health, Inc. 12
Carestream DRX-Evolution Carestream Health, Inc. 10

Showing 12 of 138. All products under System, X-Ray, Stationary

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231995 2023-10-25
K193360 2020-01-02

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