Who else makes this device?

Name: Table RAD CS
Brand: Table RAD CS

Table RAD CS

Catalogue number 10273205, listed by Siemens Healthcare Limited, Canada, under Table, Radiologic. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26

4manufacturers in China registered for this device type

1catalogue number

3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (1), Shanghai (1), Tianjin (1).

Chinese manufacturers registered for FDA product code KXJ
Manufacturer	City	Province	Registered as	Device types
GE Healthcare (China) Co., Ltd.	Beijing	Beijing	Specification developer	22
Carestream Health, Inc., Global R&D Center	Shanghai	Shanghai	Specification developer	8
GE Healthcare (Tianjin) Company Limited	Tianjin	Tianjin	Specification developer	5
Baxter Medical Systems (Suzhou) Co., Ltd.	Taicang	Jiangsu	Contract manufacturer	4

Record

Regulatory record for Table RAD CS
Listed by	Siemens Healthcare Limited, Canada
FDA product code	KXJ
Device type	Table, Radiologic
Device class	Class 2
Regulation	21 CFR 892.1980
Establishment	Contract manufacturer, Manufacturer, Exporter
Premarket notification	Exempt
Record published	2017-02-02
Record revised	2021-11-18 (version 4)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Prescription	Prescription only
Label carries	serial number
Storage	Handling environment atmospheric pressure 80 to 106 KiloPascal; Handling environment temperature 10 to 35 °C; Handling environment humidity 20 to 75 % RH

Catalogue Numbers

Catalogue numbers for Table RAD CS
Catalogue number	Size	Status
10273205		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Tidi	Tidi Products, LLC	1,329
Table, Radiologic	Domico Med-Device, LLC	351
Hillrom™	Baxter Medical Systems GmbH + Co. KG	167
Trumpf Medical	Baxter Medical Systems GmbH + Co. KG	118
Scancoat	Domico Med-Device, LLC	82
Gems	Tidi Products, LLC	71
Pads	Baxter Medical Systems GmbH + Co. KG	41
Bone Foam	Tidi Products, LLC	25
TS 7500	Baxter Medical Systems GmbH + Co. KG	21
Orthopedic Extension	Baxter Medical Systems GmbH + Co. KG	19
Bionix	Tidi Products, LLC	16
Control Units	Baxter Medical Systems GmbH + Co. KG	11

Showing 12 of 107. All products under Table, Radiologic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K820111	1982-02-18
K790783	1979-05-07
K781992	1978-12-07

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.