Crest Medical Limited
Crest Medical: Ein führender Lieferant und Hersteller von hochwertigen Erste-Hilfe-Sets, Arbeitsschutzprodukten, persönlicher
Crest Medical: Ein führender Lieferant und Hersteller von hochwertigen Erste-Hilfe-Sets, Arbeitsschutzprodukten, persönlicher Schutzausrüstung (PSA) und Verbrauchergesundheitslösungen
- Type
- brand seeking distribution
- Location
- Warrington, United Kingdom
- Founded
- 1999
- Website
- crestmedical.co.uk
- Categories
- Medizin- & Gesundheitsbedarf, Sicherheits- & Schutzausrüstung
Listed in a source registry
PLMA Private Label Trade Show 2026 exhibitor directory (Chicago)
Verified facts
- lei-lapsed (amber), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registered-since (green), checked 1999-11-15 Companies House free company data product (UK)
- licensed-sponsor (green), checked 2026-08-12 UK Home Office register of licensed sponsors (workers)
- debarment-clear (green), checked 2026-09-03 OpenSanctions
- domain-registered (green), checked 2026-09-03 Domain registry record
- sanctions-clear (green), checked 2026-09-03 OpenSanctions
- fda-registered (green), checked 2026-09-03 FDA
- directors-on-file (green), checked 2026-07-09 Companies House
- corporate-mail-on-domain (green), checked 2026-09-03 Mail server of the company domain
- registered-trade-role (green), checked 2026-08-01 MHRA register of licensed manufacturing and wholesale dealer sites (UK)
- ch-active (green), checked 2026-07-09 Companies House
- registered-trade-only (amber), checked 2026-07-09 Companies House
- public-contract-awarded (green), checked 2026-08-16 Contracts Finder: awarded public contracts (UK Cabinet Office) Hier trägt der Zuschlag zusätzlich eine fremde Prüfung: Im Vereinigten Königreich muss der Auftraggeber Lieferanten ausschließen, auf die zwingende Ausschlussgründe zutreffen, darunter Verurteilungen wegen Betrugs, Korruption, Steuerstraftaten und Verstößen am Arbeitsmarkt. Procurement Act 2023, Schedule 6 (mandatory exclusion grounds)
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)
- Protective equipment (helmets, gloves, eyewear) sold in the EU falls under the PPE Regulation (EU) 2016/425 and needs CE marking. European Commission (PPE)