This resource reflects an instance of a biologically derived product. A material substance originating from a biological entity intended to be transplanted or infused into another (possibly the same) biological entity.

Substances include, but are not limited to: whole blood, bone marrow, organs, and manipulated blood cells.

This records identifiers associated with this biologically derived product instance that are defined by business processes and/or used to refer to it when a direct URL reference to the resource itself is not appropriate (e.g. in CDA documents, A category or in written / printed documentation). classification of the product. Products may be assigned multiple categories, for example a human heart valve can be categorized as an 'MPHO' and 'tissue'.

Broad category A codified value that systematically supports characterization and classification of this product. medical products of human origin inclusive of processing conditions such as additives, volumes and handling conditions.

A code that identifies the kind of this biologically derived Parent product (SNOMED Ctcode). (if any) for this biologically-derived product.

For products that have multiple collections. For example Peripheral Blood Stem Cells may be collected over several days from a single donor and the donation split into in multiple containers which must be linked to the parent donation.

Procedure request Request to obtain and/or infuse this biologically derived product.

Number of discrete units within this Unique instance identifiers assigned to a biologically derived product. Note: This is a business identifier, not a resource identifier.

This identifier should uniquely identify the product instance in the business domain. Ideally it should be a globally unique identifier under the control of an ISO/IEC 15459 Issuing Agency.

Parent An identifier that supports traceability to the event during which material in this product (if any). from one or more biological entities was obtained or pooled.

For products Necessary to support mandatory requirements for traceability from donor/source to recipient and vice versa, while also satisfying donor anonymity requirements. The element is defined consistently across BiologicallyDerivedProduct, NutritionProduct, and Device. The identifier references an event that have links to a single biological entity such as a blood donor, or to multiple collections. For example Peripheral Blood Stem Cells biological entities (e.g. when the product is an embryo or a pooled platelet product). A single biologicalSourceEvent identifier may be collected over several days appear on multiple products of many types derived from a single donor and the donation split into in event or source extraction. As an example, a single donation event may provide 2 kidneys and a liver for organ transplantation, 2 corneas for eye surgery, heart valves and arterial tissue for cardiovascular surgery, multiple containers which must skin grafts, tendons, multiple shaped bone grafts and a large number of bone putty/paste products; and each of them may be linked assigned to the parent donation. same biological source event identifier.

How Processing facilities responsible for the labeling and distribution of this product was collected. biologically derived product.

Healthcare professional who is performing A unique identifier for an aliquot of a product. Used to distinguish individual aliquots of a product carrying the collection. same biologicalSource and productCode identifiers.

The patient or entity, such as a hospital or vendor in the case current status of a processed/manipulated/manufactured product, providing the product.

Time Date, and where relevant time, of product collection. expiration.

Any processing of the How this product during collection that does not change the fundamental nature of the product. For example adding anti-coagulants during the collection of Peripheral Blood Stem Cells. was collected.

Description of of processing. Healthcare professional who is performing the collection.

Procesing code. The patient providing the product.

The collection.source may reference an identifiable patient. Implementers shall ensure the appropriate data access controls are established.

Substance added during processing. The entity, such as a hospital or vendor in the case of a processed/manipulated/manufactured product, providing the product.

Time of processing. product collection.

Any manipulation of product post-collection that is intended The procedure performed to alter collect the biologically derived product. For example a buffy-coat enrichment or CD8 reduction of Peripheral Blood Stem Cells to make it more suitable for infusion.

Time The temperature requirements for storage of manipulation. the biologically-derived product.

Product storage. May be extracted from information held in the productCode element.

Description of storage. A property that is specific to this BiologicallyDerviedProduct instance.

Storage temperature. Property can be used to provide information on a wide range of additional information specific to a particular biologicallyDerivedProduct.

Temperature scale used. Code that specifies the property. It should reference an established coding system.

The element is identified by name and system URI in the type. Some types may have multiple occurrences.

Storage timeperiod. Property values.

The value should be provided as a boolean, integer, CodeableConcept, period, quantity, range, ratio, or attachment. The description can be a string only when these others are not available.