Instructions for Statics & Installation

Planning and building code requirements, as well as static tests, remain the responsibility of the buyer and must be verified before installation begins. Individual national and regional building odes must be considered. All products must be installed in accordance with commonly stablished echnical rules.

Delivery does not include mounting parts for product installation as these depend on various static requirements. The operating instructions and safety instructions must be observed and complied with instructions for use must be kept in accordance with the legal regulations. Should the instructions for use not be enclosed by mistake, please contact us in any case.

Application of accessories

Always follow the instructions in the operating manuals of the product, when using accessories. If necessary, the maximum load of the accessories and the basic product must be reduced due to local conditions or the special configuration. In these cases there is no warranty granted by provita medical gmbh & co. kg. The compliance to the standards and regulations, especially the MPBetreibV (operator regulation) is the responsibility of the customer/user.

If you attach provita accessories to third party products or mount third party products to provita products, a new complete system may be created. The operator shall be then responsible for the evaluation and liability is then incumbent on the operator.

Installation of accessories

Generally when installing accessories and other parts,

it is important to consider that:

the mounting options are adapted to the product
add-on components are firmly and securely attached
the assembly of attachments does not create danger and potentially risks
the balance point of the systems does not shift unfavourable (by offload parts)
valid standards and guidelines are met (DIN ISO 60601, 3rd Edition, MPG, MPBetreibV)

Accessories for IV-Poles

We would like to emphasize that not all bottle holder/ - bar - models/ accessories are suitable for products with none weighted base constructions. For safety reasons, we would like to suggest to take advantage of the opportunity to get professional guidance by our competent sales team experts in regards to “tilting safety“ and the standard requirements of DIN EN 60601. Also changes done to the products jeopardise the approval in accordance with DIN EN 60601. Gladly we will provide consulting also in this matter.

Accessories for Wall and Ceiling Rails

When using accessories for Wall- and Ceiling Rail Systems, the specified maximum load capacity in the assembly instructions must be observed. The load capacity of the wall / ceiling must be calculated so that the input forces exerted by the rails can be absorbed. Relevant safety factors have to be considered. If applicable, static examinations are necessary.

General Product Information

provita products must only be used in accordance with their intended purpose, and in compliance with applicable statutory provisions, according to commonly accepted technical rules. They must be installed, operated and maintained in accordance with applicable work safety and accident prevention regulations.

They must be installed, operated, and maintained solely by persons with the appropriate training, and adequate knowledge and experience.

Before using any provita product, the user must ascertain its proper functionality and the conditions for effective application of the medical product. The user must also pay attention to the operating manual and other miscellaneous safety-related information and maintenance notes delivered with the product. A provita product operator must only charge persons, companies or institutions with the maintenance (maintenance, inspection, repair and reconditioning) of medical products, where the individuals concerned have the required technical knowledge, fulfill the necessary conditions, and have the necessary means to properly discharge such duties.

Upon maintenance or repair of medical products, the primary constructional and functional product features relevant to safety and operability must be inspected, in as far as they may have been affected by the maintenance activities performed.

Where safety-related inspections are not mandated, but at the same time are not expressly excluded, the operator shall, in accordance with generally accepted rules of the trade, perform or have such safety-related inspections performed at timely intervals, to enable the detection of any defects that may be expected in the light of past experience. The interval for such inspections shall, however, not exceed a period of two years.

An inspection log is to be created for these safety inspections, detailing the date of inspection and any evaluations made. The operator shall retain such logs at least until the subsequent safety inspection. If a product is damaged or if there is any doubt as to its complete functionality, the product must not be used under any circumstances. In such specific cases, please feel free to contact us.

Disclaimer

provita medical’s product liability shall be limited to the statutory liability requirements for the advertised characteristics of products contained in this catalogue. Any further liabilities – particularly for products from third parties listed in this catalogue - are excluded.

Trademarks

The products depicted in this catalogue may be under patent or subject to intellectual property rights. The reproduction of trademarked products constitutes a breach of the law, and may result in liability for damages. The information and illustrations in this catalogue do not release the user from the obligation to independently establish whether claims could arise from third party intellectual property rights.

Copyright provita medical gmbh & co. kg, 2024
Reproduction and duplication (even in excerpts) are not permitted without the permission of provita medical gmbh & co. kg.

For more than 50 years, our family business has been one of the leading manufacturers in medical technology.

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