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
- 의료 및 건강 관리 용품, 안전 및 보호 장비
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) 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. 영국에서는 발주기관이 필수 배제 사유에 해당하는 공급자를 반드시 배제해야 하며, 그 사유에는 사기, 부패, 조세 범죄, 노동시장 침해에 대한 유죄판결이 포함됩니다. 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)