Why DataMatrix Code?
A device that is marked with information such as the serial number or expiration date is easily traceable, and thus its life cycle is transparent to hospitals and doctors. This so called Unique Device Identification (UDI) increases patient safety and, for example, simplifies product recalls.
To mark its devices, Olympus uses DataMatrix Code (DMC), stored directly on all Class I and II products.
Each UDI consists of a unique set of article numbers for all manufacturers, named the Global Trade Item Numbers (GTINs). As components of the GS1 standards*, GTINs identify the manufacturer and the product.
The UDI with all relevant information about the device is stored in the publicly accessible Global UDI Database (GUDID). GUDID is already supplied with relevant background information by Olympus, so hospitals and doctors can use data from this database to identify products.
*see glossary at the bottom of the page
The Benefits of Direct Part Marking (DPM) with UDI A permanently marked and thus uniquely identifiable and traceable product possesses various benefits for hospitals and doctors:
Frequently Asked Questions
The UDI includes the following elements:
- GTIN – a world unique item number
- (11) Production Date – for reusable and unsterile items only
- (21) Serial Number (SN) – assigned by Olympus
Example: (01)12345678910111(11)170105(21)WA123456
- GTIN – a world unique item number
- (17) Expiration Date – for sterile products only
- (10) Batch Number (LOT) – assigned by Olympus
Example: (01)12345678910111(17)170105(10)WA123456
For the DPM of a batch-managed product, the UDI may be supplemented with an additional non-UDI element:
- (91) Batch Number Annex
Yes, comprehensive product information is accessible via the Global UDI Database (GUDID).
According to regulatory criteria the following exceptions exist:
1. Single-use devices.
2. If one parent device bears UDI, the other devices including the configurable medical device system may not bear Direct Part Marking.
3. Markings that could interfere with the safety or effectiveness of the device.
4. If it's not technical feasible.
Glossary
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