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, MEDICAL EQUIPMENT AND CONSUMABLES
コンテンツへスキップ EIRA MED 血液サービス向けの自社生産 設備と流通 EiraMed は、医療製品を生産するための最新の製薬複合施設です 詳細はこちら 自社生産 同社が生産する主な製品は、血液とその成分用のポリマー容器です。この製品、および血液成分の分離と消毒のために工場で製造されるハイテクフィルターやシステムの主な消費者は、共和国全土の血液センターです。設備 自動ドナー血漿交換装置 Haemonetics PCS2、細胞質血漿交換装置 MCS+、Haemonetics (米国) 製自動細胞処理装置 ACP215、照射装置 INTERCEPT 照明装置 CERUS 製 Distribution SSP+ ソリューション、クライオバッグ、An
- 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
- 医療およびヘルスケア用品
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)