O‘zbekiston Raqamli sog‘liqni saqlash platformasi
0.12.0 - ci-build
O‘zbekiston Raqamli sog‘liqni saqlash platformasi
0.12.0 - ci-build
Uzbekistan Digital Health Platform, Ministry of Health of the Republic of Uzbekistan tomonidan e’lon qilingan. Ushbu qo‘llanma rasmiy nashr emas; u FHIR (HL7® FHIR® Standard) CI Build tomonidan yaratilgan 0.12.0 versiyasi uchun uzluksiz yig‘ma hisoblanadi. Ushbu versiya https://github.com/uzinfocom-org/digital-health-ig/ dagi joriy kontentga asoslangan va muntazam ravishda o‘zgarib turadi. Nashr etilgan versiyalar katalogini ko‘ring
| Rasmiy URL: https://terminology.dhp.uz/fhir/core/ValueSet/device-name-type-vs | Versiya: 0.12.0 | ||||
| Draft 2026-11-02 holatiga ko‘ra | Kompyuterda qayta ishlanadigan nom: DeviceNameTypeVS | ||||
Device name types
References
Ushbu ValueSet kod tizimi qo‘shimchasini talab qiladi Device name type translations.
http://hl7.org/fhir/device-nametype versiya 📍5.0.0
Expansion ichki tarzda quyidagiga asoslanib bajarildi:
Ushbu qiymatlar to‘plami 3 ta conceptni o‘z ichiga oladi
| Tizim | Code | Ko‘rsatiladigan qiymat (uz) | Ta'rif | JSON | XML |
http://hl7.org/fhir/device-nametype | registered-name | Ro'yxatdan o'tgan nomi | The term assigned to a medical device by the entity who registers or submits information about it to a jurisdiction or its databases. This may be considered the manufacturer assigned name (e.g., brand name assigned by the labeler or manufacturer in US, or device name assigned by the manufacturer in EU) and may also be synonymous with proprietary name or trade name of the device. | ||
http://hl7.org/fhir/device-nametype | user-friendly-name | Foydalanuvchiga qulay nomi | The term that generically describes the device by a name as assigned by the manufacturer that is recognized by lay person. This common or generic name may be printed on the package it came in or some combination of that name with the model number, serial number, or other attribute that makes the name easy to understand for the user of that device. It is often exposed in communicating devices transport protocols. It is provided to help users identify the device when reported in discovery operations. | ||
http://hl7.org/fhir/device-nametype | patient-reported-name | Bemor tomonidan bildirilgan nom | the term used by the patient associated with the device when describing the device, for example 'knee implant', when documented as a self-reported device. |