TECNICAS RADIOFISICAS S.L.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Tecniche Radiofisiche Vai al contenuto Tecniche Radiofisiche - Rendere la Medicina Sicura Esperti in Fisica Medica e Protezione Radiologica Radiophysical…
Tecniche Radiofisiche Vai al contenuto Tecniche Radiofisiche - Rendere la Medicina Sicura Esperti in Fisica Medica e Protezione Radiologica Radiophysical Techniques è un'azienda spagnola presente in più di 20 paesi in tutto il mondo specializzata nello sviluppo di soluzioni personalizzate per il campo della radioterapia, della medicina nucleare e della radiodiagnosi. contattaci Quattro decadi nel settore ci hanno reso un punto di riferimento nella progettazione di impianti radioattivi in campo medico, nonché nella realizzazione di prodotti destinati all'utilizzo in ambienti con radiazioni ionizzanti. Consulenza Progettiamo soluzioni su misura, adatte ad ogni installazione e normativa. Produzione Sviluppiamo attrezzature che uniscono innovazione, sicurezza e qualità.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Zaragoza, Spain
- Website
- https://trf.es
- Categories
- Forniture medicali e sanitarie
- Markets
- Spagna
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 2 official sources are on file. 3 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-23. Mail server of the company domain
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-23. OpenSanctions
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-08-23. GLEIF
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-23. OpenSanctions
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-03. ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
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)