Stryker Model 1501 Stretcher Manual

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Stryker Model 1501 Stretcher Manual

Stryker 1115 Stretcher Parts Diagram
Stryker Model 1501 Stretcher Manual Instructions
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Stryker 1115 Stretcher Parts DiagramCleaning Model 1231/1731 stretchers are designed to be power–washable. The unit may show some signs of oxidation or discoloration from continuous washing. However, no degradation of the stretcher's performance charac- teristics or functionality will occur due to power washing as long as the proper procedures are followed. Page 19: Cleaning. Stretcher Parts Manual 1501 Stryker Stretcher Parts Manual Getting the books 1501 stryker stretcher parts manual now is not type of inspiring means You could not single-handedly going similar to ebook buildup or library or borrowing from your associates to edit them This is an entirely easy.
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 Class 2 Device Recall Stryker stretcher, Model 1501.
Date Initiated by FirmNovember 15, 2004
Date PostedNovember 10, 2007
Recall Status1Terminated 3 on October 27, 2010
Z-0235-2008
Recall Event ID37214
Stretcher - Product CodeFPO
ProductStryker Renaissance Series/Advantage Series PACU wheeled stretcher, Model 1501, Stryker Medical, Portage, MI 49002
Code InformationAll stretchers with serial numbers beginning with 0309 through 0505.
Recalling Firm/
Manufacturer Stryker Medical Div. of Stryker Corporation
 3800 E. Centre Ave.
 Portage MI 49002
For Additional Information Contact
800-669-4968 Ext. 6689 
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. 
Component change control
The firm issued an Urgent Medical Device Correction Letter dated 9/24/07, to each consignee informing them of the problems, that the brakes on each affected stretcher needed to be inspected/tested and removed from service if brake problems were discovered, and that a Stryker service representative would be in contact to replace the brakes.
81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models.
Worldwide-USA, Argentina, Australia, Brazil, Canada, Chile, China, Dubai, France, India, Italy, Japan, Germany, Greece, Hong Kong, Korea, Latin America, Malaysia, Mexico, Netherlands, Poland, Portugal, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, and United Kingdom.
TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. 
Overall Length: 83' (210.8 cm)
 Overall Width (siderails up): 34 ½' (87.6 cm)
 Overall Width (siderails down): 30 ½' (77.5 cm)
 Height Overall – High Position: 35 ½' (90.2 cm)
 Height Overall – Low Position: 22' (55.9 cm)
 Patient Surface: 29' x 76' (73.7 cm x 193 cm)
 Siderails:14' x 54' (35.6 cm x 137 cm)
 Caster Size: 8' (20.3 cm)
 Knee Gatch: 0° – 30°
 Backrest: 0° – 90°
 Trendelenburg/Reverse Trendelenburg: ±18°
 Maximum Patient Weight: 500 lb. (226.8 kg)
At Piedmont Medical, we are committed to our responsibility to our clients. Our after-sales service is designed to provide the highest degree of satisfaction.
Matthew WurdemanPresident/Sales Representative
Matthew@piedmontmedicalinc.com
Woody Wurdeman
Elisa OntiverosAdministration/Spanish Translator
Elisa@piedmontmedicalinc.com

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