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
- 医療およびヘルスケア用品, 安全および保護装置
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) ここでの落札は、他者による審査も伴います。英国では、発注機関は強制的除外事由に該当する供給者を排除しなければならず、その事由には詐欺、汚職、租税犯罪、労働市場での違反による有罪判決が含まれます。 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)