Crest Medical Limited
Crest Medical: A Leading Supplier and Manufacturer of High-Quality First Aid Kits, Occupational Health Products, Personal Protective
Crest Medical: A Leading Supplier and Manufacturer of High-Quality First Aid Kits, Occupational Health Products, Personal Protective Equipment (PPE), and Consumer Health Solutions
- Type
- brand seeking distribution
- Location
- Warrington, United Kingdom
- Founded
- 1999
- Website
- crestmedical.co.uk
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, सुरक्षा एवं सुरक्षा उपकरण
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) यहाँ ठेका मिलना किसी और की जाँच भी साथ लाता है: ब्रिटेन में क्रय संस्था को उन आपूर्तिकर्ताओं को बाहर करना अनिवार्य है जो अनिवार्य बहिष्करण आधारों में आते हैं, जिनमें धोखाधड़ी, भ्रष्टाचार, कर अपराध और श्रम बाजार में दुरुपयोग की दोषसिद्धि शामिल है। 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)