SonoSite SII

19 catalogue numbers from P23620-14R, listed by Fujifilm Sonosite,inc., United States, under Transducer, Ultrasonic, Diagnostic. 44 manufacturers in China are registered for this product code.

Registry build 21.09.26
44manufacturers in China registered for this device type
19catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Guangdong (18), Jiangsu (10), Shanghai (3). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ITX
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Ming FAI Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 17
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Hony Medical Co., Ltd. Taishan Guangdong Contract manufacturer 10
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Showing 12 of 44. All 44 manufacturers in China registered for Transducer, Ultrasonic, Diagnostic

Record

Regulatory record for SonoSite SII
Listed by Fujifilm Sonosite,inc., United States
FDA product code ITX
Device type Transducer, Ultrasonic, Diagnostic
Device class Class 2
Regulation 21 CFR 892.1570
Establishment Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K160734
Record published 2017-12-27
Record revised 2018-07-06 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment humidity 15 to 95 % RH; Handling environment temperature -20 to 60 °C; Storage environment temperature -20 to 60 °C; Storage environment atmospheric pressure 50 to 106 KiloPascal; Handling environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 15 to 95 % RH

Catalogue Numbers

Catalogue numbers for SonoSite SII
Catalogue number Size Status
P23620-14R In distribution
P20500-10 In distribution
P30381-02 In distribution
P23630-14 In distribution
P23620-13 In distribution
P24550-46R In distribution
P23620-45 In distribution
P23630-14R In distribution
P24550-45 In distribution
P23630-13 In distribution
1 In distribution
P20500-13R In distribution
P20883-10 In distribution
P24550-46 In distribution
P23630-13R In distribution
P24550-03R In distribution
P24550-01 In distribution
P24550-41R In distribution
P20500-13 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SonoScape Sonoscape Medical Corp. 302
Biopsy Starter Kit Civco Medical Instruments Co., Inc. 172
Sheathes Sheathing Technologies, Inc. 170
Needle Guide Civco Medical Instruments Co., Inc. 156
Sheathes3D Sheathing Technologies, Inc. 78
Ultrasound Probe Cover Biopsy Needle Guide Advance Medical Designs, Inc. 78
ultrasonic transducer Edan Instruments, Inc. 70
Unbranded Advance Medical Designs, Inc. 68
Reusable Biopsy Bracket Protek Medical Products, Inc. 60
Ultrasound Probe Cover Biopsy Needle Guide Kit Advance Medical Designs, Inc. 58
Biopsy Bracket Civco Medical Instruments Co., Inc. 56
Transducer Cover Civco Medical Instruments Co., Inc. 54

Showing 12 of 1,678. All products under Transducer, Ultrasonic, Diagnostic

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2005-12-12 Not classified Other 22 gauge needle guides were intermixed with 21 gauge guides and labeled as 21 gauge needle guides. 355 boxes/24 kits per box 2006-07-31

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