Stryker Mul-T-Pad 8002-062-612 Operation Manual Download Page 1

Stryker Medical, a division of Stryker Corporation (“Stryker”) warrants that its 

models

 

8002-062-612, 8002-062-622, and 8002-062-626 

Mul-T-Pad 

products 

will be free from defects in manufacturing and workmanship for a maximum 

of 30 day use period. “Use” period begins when such devices individual 

package is opened. Stryker’s obligation under this warranty is expressly limited 

to supplying a product replacement, at its option, any product which is, in 

the sole discretion of Stryker, found to be defective. If requested by Stryker, 

products for which a claim is made shall be returned prepaid to the factory. 

Any improper use or any alterations or repair by others in such manner as in 

Stryker’s judgement affects the product materially and adversely shall void this 

warranty. Any repair of Stryker products using parts not provided or authorized 

by Stryker shall void this warranty. No employee or representative of Stryker is 

authorized to change this warranty in any way.

Warranty exclusion and damage limitations

The express warranty set forth herein is the only warranty applicable to the 

product. 

Any and all other warranties, whether express or implied, including 

any implied warranty of merchantability or fitness for a particular purpose 

are expressly excluded by Stryker.

 In no event shall Stryker be liable for 

incidental or consequential damages.

Return authorization

Product cannot be returned without prior approval from the Stryker Customer 

Service Department. An authorization number will be provided which must be 

printed on the returned product. Stryker reserves the right to charge shipping 

and restocking fees on returned product. Special, modified, or discontinued 

products are not subject to return.

Damaged merchandise

ICC Regulations require that claims for damaged product must be made with 

within fifteen (15) days of receipt of the product. Do not accept damaged 

shipments unless such damage is noted on the delivery receipt at the time 

of receipt. Upon prompt notification, Stryker will file a freight claim with the 

appropriate carrier for damages incurred. Claims will be limited in amount to 

the actual replacement cost. In the event that this information is not received by 

Stryker within the fifteen (15) day period following the delivery of the product, 

or the damage was not noted on the delivery receipt at the time of receipt, the 

customer will be responsible for payment of the original invoice in full within 

thirty (30) days of receipt. Claims for any incomplete shipments must be made 

within thirty (30) days of invoice.

International warranty clause

This warranty reflects U.S. domestic policy. Warranty outside the U.S. may 

vary by country. Please contact your local Stryker Medical representative for 

extra information.

General warning

Caution

Consult instructions for 

use

Do not puncture

Quantity

1

Single patient use

Batch code

Catalogue number

Date of manufacturer

Manufacturer

Symbols

Operations Manual

2014/12 B.0

8002-009-131 REV B

www.stryker.com

Warranty

2014/12

8002-009-131 REV B

www.stryker.com

Stryker Medical
3800 E. Centre Avenue
Portage, MI  49002
USA

Operation

Mul-T-Pad

®

 

8002-062-612
8002-062-622
8002-062-626

 WARNING

• 

Do not use if the package is damaged.

• 

Always use 

Mul-T-Pad 

products with an approved temperature controller. 

Using this product with other controllers has not been tested.

• 

Do not reuse this product on another patient to avoid the risk of cross-
contamination and infection.

• 

Do not use this product to position or transfer a patient.

• 

Do not allow hoses to fold, kink, or to wrap around a patient.

• 

Always pre-fill the pad before applying to the patient.

• 

Always check the patient’s skin condition of areas in contact with the 
pad at a minimum of 30 minutes or as directed by a physician.

• 

Always consult the controller operations manual before connecting this 
product.

 CAUTION

• 

US Federal Law restricts this device to sale by or on the order of a 

licensed physician.

• 

Do not use sharp objects or pins with this product.

• 

Do not clean this product. If soiled, dispose of product according to 

hospital protocol. This is a single patient use product.

• 

Always inspect the product for tears, cuts, holes, stains, or any other 

damage before use. Always monitor more frequently pediatric patients 

and patients with impaired circulation.

• 

Always use minimal layers of sheeting and incontinence pads. Too many 

layers between the patient’s skin and the pad will reduce the cooling or 

warming capabilities of the system.

Disposing of the product

Dispose of the product in accordance with your local waste management 

policy.

Safety Precautions

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