Power-PRO 2, High Configuration – No Wifi

Catalogue number 650705550003, listed by Stryker GmbH, Switzerland, under Stretcher, Wheeled. 31 manufacturers in China are registered for this product code.

Registry build 21.09.26
31manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (15), Hebei (7), Guangdong (6). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FPO
Manufacturer City Province Registered as Device types
Hengshui Gangsheng Medical Instruments Co., Ltd. Hengshui Hebei Contract manufacturer 36
Zhangjiagang Xiehe Medical Apparatus & Instruments Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Hospital & Homecare IMP. & EXP. Co., Ltd. Nanjing Jiangsu Contract manufacturer 179
Danyang NEW Hope Medical Equipment Co., Ltd. Danyang Jiangsu Manufacturer 38
Jiangsu Saikang Medical Equipment Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 34
Jiangsu Yongfa Medical Equipment Technology Co., Ltd. Zhangjiagang Jiangsu Manufacturer 33
Shanghai NO. 2 Medical College Duhang Medical Equipment Factory Shanghai Shanghai Contract manufacturer 32
Jiangsu Rooe Medical Technology Co., Ltd. Zhangjiagang Jiangsu Manufacturer 31
Better Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 24
Shenyang Ourpromise Medical Equipment Co., Ltd. Shenyang Liaoning Manufacturer 24
Foshan Fuzikon Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 21
Jiangsu Sintang Health&Technology Co., Ltd. Yancheng Jiangsu Manufacturer 21

Showing 12 of 31. All 31 manufacturers in China registered for Stretcher, Wheeled

Record

Regulatory record for Power-PRO 2, High Configuration – No Wifi
Listed by Stryker GmbH, Switzerland
FDA product code FPO
Device type Stretcher, Wheeled
Device class Class 2
Regulation 21 CFR 880.6910
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2021-09-20
Record revised 2023-06-12 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number
Storage Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment temperature -30 to 130 °F; Handling environment temperature -30 to 130 °F; Handling environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 10 to 93 % RH; Handling environment humidity 10 to 93 % RH

Catalogue Numbers

Catalogue numbers for Power-PRO 2, High Configuration – No Wifi
Catalogue number Size Status
650705550003 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sechrist Industries, Inc. Sechrist Industries, Inc. 51
Stretcher, Wheeled Gendron, Inc. 40
Stretcher, Wheeled Stryker GmbH 35
Havasu Stryker GmbH 29
MJM 900 Series Gurney M J M International Corporation 27
Sprint 100 L I N E T spol. s r.o. 27
Hausted GF Health Products, Inc 24
Mondial® Monobloc Ferno-Washington, Inc. 24
Mondial® Transporter Ferno-Washington, Inc. 20
Prime Series Stryker GmbH 18
Pedigo Products, Inc. Pedigo Products, Inc. 15
Zephyr Patient Stretcher Diacor, Inc. 14

Showing 12 of 182. All products under Stretcher, Wheeled

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113598 2011-12-20
K942948 1995-01-24
K943864 1994-08-25
K935297 1994-02-18
K920704 1992-03-23

Recalls

14 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
2023-05-24 Class II Process control Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion. 1,980 cots
2023-02-01 Class II Under Investigation by firm Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloadi 4 units
2022-11-11 Class II Under Investigation by firm Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected. 465 (403 US; 62 OUS)
2021-05-12 Class II Under Investigation by firm Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the
correct use environment, but home users may not b
1 unit
2021-05-12 Class II Under Investigation by firm Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the
correct use environment, but home users may not b
3 units
2021-05-12 Class II Under Investigation by firm Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the
correct use environment, but home users may not b
3 units
2018-11-20 Class II Under Investigation by firm The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be
broken.
3285 2020-07-09
2018-03-12 Class II Nonconforming Material/Component The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken. 4724 2020-05-12
2018-03-09 Class II Labeling Change Control The Operations Manual and Maintenance Manual are missing various warnings and contain incorrect information. 59 2019-04-09
2018-03-09 Class II Labeling Change Control The Operations Manual and Maintenance Manual are missing various warnings and contain incorrect information. 3 2019-04-09
2016-11-08 Class II Under Investigation by firm Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot Fasteners due to complaints that fastening system may not have been securely fastened or had an inability to fasten into the Performance-LOAD and bounced back duri 749 units 2018-01-16
2016-05-05 Class II Vendor change control Complaints of smoke coming from the foot end of the cot. This reportedly occurred when either the battery was placed into the cot or shortly after placing the battery into the cot. In addition to the alleged smoking, one of the reports had 770 2017-09-18
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
2012-10-11 Class II Component design/selection Model 6390 Power-LOAD systems built between September 12, 2012 and September 27, 2012 may have been built with a load switch slide that does not meet specifications causing the lifting ability of the arms to be negatively impacted. 24 2013-08-30
2011-07-19 Not classified Nonconforming Material/Component The firm has determined that the brake rod assemblies of various stretchers that were built with a 5th wheel were manufactured with roll pins that did not meet the materials specifications. Some roll pins may have fractured during the asse 6 2013-08-29
2011-07-19 Not classified Nonconforming Material/Component The firm has determined that the brake rod assemblies of various stretchers that were built with a 5th wheel were manufactured with roll pins that did not meet the materials specifications. Some roll pins may have fractured during the asse 80 2013-08-29
2011-07-19 Not classified Nonconforming Material/Component The firm has determined that the brake rod assemblies of various stretchers that were built with a 5th wheel were manufactured with roll pins that did not meet the materials specifications. Some roll pins may have fractured during the asse 10 2013-08-29
2011-07-19 Not classified Nonconforming Material/Component The firm has determined that the brake rod assemblies of various stretchers that were built with a 5th wheel were manufactured with roll pins that did not meet the materials specifications. Some roll pins may have fractured during the asse 5 2013-08-29
2011-07-19 Not classified Nonconforming Material/Component The firm has determined that the brake rod assemblies of various stretchers that were built with a 5th wheel were manufactured with roll pins that did not meet the materials specifications. Some roll pins may have fractured during the asse 11 2013-08-29
2010-05-15 Not classified Device Design The firm has received 42 complaints regarding the head end lock rod, head end slide tube, brushing, and upper cross tube failures. 7,314 2012-02-07
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 4736 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 75 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 1061 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 241 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 490 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 1213 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 8825 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 196 2010-10-29
2009-08-10 Not classified Nonconforming Material/Component The brake/steer pedal may seize, resulting in the brakes not working. 970 2010-10-29
2009-02-27 Not classified Device Design The head section backrest (fowler) may not raise up, or, if up, may drop suddenly due to wearing out of the actuator threads on the fowler. 3607 2011-04-25
2009-02-27 Not classified Device Design The head section backrest (fowler) may not raise up, or, if up, may drop suddenly due to wearing out of the actuator threads on the fowler. 38 2011-04-25
2007-05-07 Not classified Other The internal power cord may become damaged due to wear and, if this occurs, a shock hazard exists. 1,048 (1009 in the U.S. plus 39 international) 2008-06-11
2006-08-29 Not classified Other The head section wheel assembly may flex outward from the cot because the head section wheel bolts, which hold the assembly upright, may back out. 1,841 cots (44 foreign) 2007-04-18
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27
2004-11-15 Not classified Component change control The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position. 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models. 2010-10-27

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