National Veterinary Services
英国の獣医薬卸売業者が全国に供給活動を行っている
National Veterinary Services (NVS) は、医薬品、消耗品、診断薬、機器、ペットの小売店を獣医診療所に販売する英国の獣医用卸売業者です。ストークオントレントの拠点から英国全土に翌日配達を提供しています。
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Stoke-on-Trent, United Kingdom
- Founded
- 2013
- Website
- https://www.nvsweb.co.uk
- Categories
- 獣医製品と動物の健康, 医療およびヘルスケア用品
- Markets
- イギリス
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-09-03 Domain registry record
- licensed-sponsor (green), checked 2026-08-12 UK Home Office register of licensed sponsors (workers)
- registered-trade-role (green), effective since 2026-08-01 MHRA register of licensed manufacturing and wholesale dealer sites (UK)
- corporate-mail-on-domain (green), checked 2026-09-03 Mail server of the company domain
- debarment-clear (green), checked 2026-09-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-09-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- directors-on-file (green), checked 2026-06-20 Companies House
- registry-active-global (green), checked 2026-09-07 Environment Agency public registers (England)
- registered-since (green), effective since 2013-04-16 Companies House free company data product (UK)
- ch-active (green), checked 2026-06-20 Companies House
- registered-trade-only (amber), checked 2026-06-20 Companies House
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)
- Veterinary medicines sold in the EU need a marketing authorisation under Regulation (EU) 2019/6, and importers need a manufacturing/import authorisation. European Medicines Agency (veterinary)