CITY TECHNOLOGY LIMITED
Sensing Solution | Honeywell
Honeywell Sensing Solutions provides a comprehensive portfolio of advanced sensing, switching, and test & measurement technologies designed to meet the diverse needs of industries such as healthcare, transportation, industrial automation, and electric vehicles. With a focus on precision and reliability, these solutions enable optimized performance across critical applications. Supported by a team of expert engineers, Honeywell ensures personalized and innovative approaches, working collaboratively with customers to deliver tailored solutions that meet their specific requirements and performance standards, driving efficiency and ensuring long-term operational success.
- Type
- Manufacturer
- Location
- PORTSMOUTH Hampshire, United Kingdom
- Founded
- 1977
- Website
- https://citytech.com
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- registry-active-global (green), checked 2026-08-24 Environment Agency public registers (England)
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- fda-registered (green), checked 2026-08-12 FDA
- fda-contract-manufacturer (green), checked 2026-08-12 FDA
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- registered-since (green), checked 1977-08-22 Companies House free company data product (UK)
- registered-manufacturer (green), checked 1977-08-22 Companies House free company data product (UK)
Claimed certifications
- FDA Registered FDA Establishment Registration
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)