DMB Apparatebau GmbH - Lohnsterilisation & Ethylenoxid Sterilisatoren
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.
DMB Apparatebau GmbH, güvenli, uygun maliyetli ve hızlı sterilizasyonun gerekli olduğu tüm alanlar için en uygun çözümü sunar. Minimal invaziv prosedürlerde kullanılanlar gibi son derece hassas ve yüksek kaliteli aletler, güvenli, güvenilir, tekrarlanabilir ve hızlı sterilizasyon süreçleri gerektirir. DMB Apparatebau GmbH, tıbbi cihaz endüstrisi, ilaç endüstrisi, klinikler gibi sağlık hizmeti sağlayıcıları ve ürünleri için güvenli, uygun maliyetli ve hızlı sterilizasyon gerektiren diğer sektörler için en uygun çözümü sağlar. Deneyimimizle istediğiniz zaman size yardımcı olabiliriz.
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Wörrstadt, Germany
- Founded
- 1955 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- dmb-apparatebau.de
- Categories
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Almanya
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. No official record 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. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- 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. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-15. OpenSanctions
- 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. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-15. OpenSanctions
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
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)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.