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Welcome to GS1 Sweden
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Industry-specific
Healthcare
Industry-specific
Construction
If I have a GTIN on products that are sold on the Swedish market, can I use the same GTIN if I want to sell the products in other countries?
Why do I need GTIN on my products?
What happens if, I for some reason, do not have GTIN as the item number on my products, will I be disqualified and excluded from the market?
What is your perspective on the existing built environment and material traceability standards?
Do we only need to put a GTIN on the base item or do we also need to put different GTINs on each pack size of the item?
What applies to assessment and certification companies?
Can we no longer use our own, or the manufacturer’s, item numbers?
Do we have to introduce data templates connected to GTIN for our products before 1 July 2022?
How does a digital product passport differ from a datasheet according to ISO 23387? Should the digital product passport be considered as a dataset within the datasheet?
Why are the Fastighetsägarna and the Swedish Construction Clients not included as requirements setters?
We are a small company with small resources and no good computer systems, so what is the least we need to do to meet this requirement?
How does GTIN relate to, for example, BEAst messaging standards – is it an opposite?
How do I know when I need to change GTIN on a product?
We manufacture products that are project-unique – ready-made windows, doors and also other carpentry. Do they require GTIN:s as well and how do we create them?
How much does GTIN cost? We are a small company and we do not have room for large increased costs?
We supply electrical and / or plumbing products that have RSK or E-numbers. Do we still need to put GTIN on our products?
We will not have time to put GTIN on our products by July 1, 2022. Who should we talk to about this?
Does this mean that you require that all product information is connected to a GTIN from 1 July 2022?
Why so urgent?
How can labeling be implemented for items such as underground drainage pipes, considering their prolonged exposure to the ground, for example in terms of recycling?
How can the validity of links in the resolver be ensured in the context of digital product passports?
As a construction client, if I require GTIN on embedded products from our contractors, is there a product database in Sweden where we can access environmental and product data?
Which standards serve as the foundation for digital product passports in terms of structure and language? Do they have any relationship with ISO 23387 and ISO 12006-3 regarding data templates and data dictionaries?
With digital product passports, the ability to scan a QR code and access a web portal with multiple links, each providing datasets owned by different actors in the value chain, arises. Is it possible to aggregate all the data from various d
Beauty
How is the trade item data handled if there are multiple distributors on the same GTIN? Is it linked to the GLN so that several suppliers can submit trade item information for the same GTIN?
What are GTIN rules?
When do I need to change the GTIN of an item and when can I keep the same GTIN?
If I as a supplier want to use different order GLNs, do I need one agreement for each order GLN?
Is there a set of regulations for measurements, for example how to measure the width of a product?
What are trade item hierarchies and trade item levels?
Guideline Trade Item Information
What is an attribute?
How do I measure an item’s height, width and depth?
The trade item’s dimensions have changed. Do I have to change GTIN?
Healthcare
What are the differences for UDI/marking for stand-alone software as opposed to physical devices?
How do I create UDI? (Medicine Technology)
Do you recommend including handling requirements such as temperature in the DataMatrix code to facilitate proper handling of the product during transport and storage?
Is the Peppol standard a solution for healthcare?
Why is it not possible to use EUDAMED as the database where healthcare retrieves its trade item information for use for orders, patient records, etc.
Is machine-to-machine transmission relevant even for a manufacturer that only has 20-30 products? After all, there are no large amounts of data to be transferred to Eudamed.
What about stand-alone software and UDI? Should readable codes be included in the label or are the numbers and link (URL) to where the code is explained sufficient.
Electricity
How do I mark my electricity meter?
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