Rhombus Castors (Malaysia) Sdn Bhd
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.
Malezyalı tıbbi-teknik tekerler, ağır hizmet tipi tekerler, taşıma ekipmanları tekerleri, aparat üreticisi
Rhombus Castors (Malezya) Sdn Bhd, Kulim, Malezya'da tıbbi-teknik tekerler, ağır hizmet tipi tekerler, taşıma ekipmanı tekerleri, aparat ve ekipman tekerleri, tekerlekler / aksesuarlar üretmektedir. Şirket 1988 yılında kurulmuş olup Malezya ve bölgesel pazarlardaki ticari müşterilere hizmet vermektedir.
- 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
- Kulim, Malaysia
- Founded
- Not established: our records disagree. 1988 in the founding-year field of our catalogue record; 1899 in the company's own website.
- Website
- rhombus.com.my
- Categories
- Mobilya, Endüstriyel Makineler, Tıbbi ve Sağlık Malzemeleri
- Markets
- Malezya, Singapur
What is established and what is not
No researcher review has been written for this company yet. No official record is on file. 1 other entry is not an official record: 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
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 2000. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-07. Internet Archive (Wayback)
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management 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)
Goods family established: Tıbbi ve Sağlık Malzemeleri (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog categories Mobilya, Endüstriyel Makineler: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.