Stretcher, Wheeled, Powered

4 catalogue numbers from 0946-044-001, listed by Stryker GmbH, Switzerland, under Stretcher, Wheeled, Powered. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
2510(k) clearances naming this product code
16recalls on this code

Who Else Makes It

All of them in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code INK
Manufacturer City Province Registered as Device types
Dragon Medical Co., Ltd. Suzhou Jiangsu Contract manufacturer 48
Yearstar Healthcare Technology Co., Ltd. Jiangyin Jiangsu Contract manufacturer 43
Zhangjiagang NEW Fellow MED Co., Ltd. Zhangjiagang Jiangsu Manufacturer 16
Jiangsu Yongxin Medical Equipment Co., Ltd. Zhangjiagang Jiangsu Manufacturer 10
Jiangyin Everise Medical Equipment Co., Ltd. Jiangyin Jiangsu Manufacturer 10

Record

Regulatory record for Stretcher, Wheeled, Powered
Listed by Stryker GmbH, Switzerland
FDA product code INK
Device type Stretcher, Wheeled, Powered
Device class Class 2
Regulation 21 CFR 890.3690
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2020-09-10

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied as a kit Yes
Label carries serial number
Storage Storage environment humidity 10 to 95 % RH; Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment temperature -4 to 140 °F

Catalogue Numbers

Catalogue numbers for Stretcher, Wheeled, Powered
Catalogue number Size Status
0946-044-001 In distribution
0390-019-000 In distribution
1105-045-100 In distribution
1010-058-000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sprint 200 L I N E T spol. s r.o. 14
Stretcher Surface Hill-Rom de México, S. de R.L. de C.V. 9
Prime Series Stryker GmbH 7
TransMotionMedical Winco Mfg., LLC 4
Sprint 400 L I N E T spol. s r.o. 3
Havasu Stryker GmbH 2
Bounder Plus 21ST Century Scientific, Inc. 1
Electric Stretcher Hill-Rom de México, S. de R.L. de C.V. 1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K140095 2014-05-20
K022309 2002-11-08

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. 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
2020-04-07 Class II Component change control Ambulance Cots may not meet crash test standard BS EN 1789 34 units 2021-01-22
2016-02-05 Class II Mixed-up of materials/components The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil used does not contain the same wear resistance additives as the specified oils and therefore i 36 2016-09-06
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 6 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 7 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 7 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 26 units 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 4 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 23 2013-08-28
2011-07-19 Not classified Nonconforming Material/Component Stryker Medical has determined that some Prime Brake Pad Assembly components were manufactured with brake shoes that did not meet specifications. Accordingly some brake shoes used within the Prime Brake Pad Assembly may wear prematurely, o 91 2013-08-28
2010-03-19 Not classified Component design/selection The retractable cord stretchers were fitted with power cords, manufactured by Electri-Cord, whose prongs have the potential to fracture inside the molded section of the plug, causing melting and charring. 238 2011-05-02
2010-03-19 Not classified Component design/selection The retractable cord stretchers were fitted with power cords, manufactured by Electri-Cord, whose prongs have the potential to fracture inside the molded section of the plug, causing melting and charring. 39 Stretchers 2011-05-02
2010-03-19 Not classified Component design/selection The retractable cord stretchers were fitted with power cords, manufactured by Electri-Cord, whose prongs have the potential to fracture inside the molded section of the plug, causing melting and charring. 19 Stretchers 2011-05-02
2010-03-19 Not classified Component design/selection The retractable cord stretchers were fitted with power cords, manufactured by Electri-Cord, whose prongs have the potential to fracture inside the molded section of the plug, causing melting and charring. 61 stretchers 2011-05-02
2010-03-19 Not classified Component design/selection The retractable cord stretchers were fitted with power cords, manufactured by Electri-Cord, whose prongs have the potential to fracture inside the molded section of the plug, causing melting and charring. 4,558 Stretchers 2011-05-02
2003-12-30 Not classified Other Users may be pinched in the siderail assembly when raising or lowering the siderail. 107 2004-04-15
2003-12-01 Not classified Other The user may be pinched by the siderail when raising or lowering the siderail. 3903 2004-04-12

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