ТОО "Eira Med" ("Эйра Мед")
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Eira Med, THIẾT BỊ Y TẾ VÀ VẬT LIỆU TIÊU DÙNG
Chuyển đến phần nội dung EIRA MED Sản xuất riêng các dịch vụ về máu Thiết bị và phân phối EiraMed là một tổ hợp dược phẩm hiện đại để sản xuất các sản phẩm y tế Tìm hiểu thêm Sản xuất riêng Sản phẩm chính do công ty sản xuất là hộp đựng polymer đựng máu và các thành phần của nó. Khách hàng chính của sản phẩm này, cũng như các bộ lọc và hệ thống công nghệ cao do nhà máy sản xuất để tách các thành phần máu và khử trùng chúng, là các trung tâm máu trên khắp Cộng hòa.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Astana, Kazakhstan
- Website
- http://wp.eiramed.kz/
- Categories
- Vật tư y tế và chăm sóc sức khỏe
Listed in a source registry
Kazakhstan, register of domestic manufacturers (e-ondiris.gov.kz)
What is established and what is not
No researcher review has been written for this company yet. 1 official record from 1 official source is on file. 2 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-09-01. OpenSanctions
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-09-01. OpenSanctions
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-08-30. Register of domestic manufacturers, Kazakhstan (e-ondiris.gov.kz)
Relationships
1 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Recorded in a source
- Konteyner Polimernyy Dlya Krovi I Eyo Komponentov Chetyryokhkamernyy S Rastvorom Gemokonservanta «CPD», Resuspendiruyushchim Rastvorom «PAGGSM» I ... (Контейнер полимерный для крови и её компонентов четырёхкамерный с раствором гемоконсерванта «CPD», ресуспендирующим раствором «PAGGSM» и ...): Products on the register. Register of domestic manufacturers, Kazakhstan (e-ondiris.gov.kz)
Candidates, not confirmed
- wp.eiramed.kz: Website of this business. Source record
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)