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Stryker Model 1501 Stretcher Manual

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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)

  1. Stryker Model 1501 Stretcher Manual For Sale
  2. Stryker 1105 Stretcher Service Manual

Manuals and User Guides for Stryker Zoom. We have 1 Stryker Zoom manual available for free PDF download: Operation Manual Stryker Zoom Operation Manual (42 pages). Cleaning 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.

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Stryker Model 1501 Stretcher Manual For Sale


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Stryker 1105 Stretcher Service Manual

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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.




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