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.
الشركة المصنعة الماليزية للعجلات الطبية التقنية، والعجلات الثقيلة، وعجلات معدات النقل، والأجهزة
Rhombus Castors (ماليزيا) تقوم Sdn Bhd بتصنيع العجلات الطبية التقنية، وعجلات الخدمة الشاقة، وعجلات معدات النقل، وعجلات الأجهزة والمعدات، والعجلات/الملحقات في كوليم، ماليزيا. تأسست الشركة في عام 1988 وتقوم بتزويد العملاء التجاريين في ماليزيا والأسواق الإقليمية.
- 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
- أثاث, الآلات الصناعية, اللوازم الطبية والرعاية الصحية
- Markets
- ماليزيا, سنغافورة
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: اللوازم الطبية والرعاية الصحية (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 أثاث, الآلات الصناعية: 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.