Frimed Medizintechnik GmbH
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.
Frimed Medizintechnik GmbH - Your Expert for Surgical Instruments from Tuttlingen For over 30 years, Frimed Medizintechnik GmbH has been located in the heart…
Frimed Medizintechnik GmbH - Your Expert for Surgical Instruments from Tuttlingen For over 30 years, Frimed Medizintechnik GmbH has been located in the heart of Tuttlingen, the world-renowned center of medical technology. Our company specializes in the supply of surgical instruments, which we offer both as OEM products and under our own name. As an established company, we have continuously grown and evolved to provide you with high-quality instruments at attractive prices. Our long-standing experience and commitment to quality have made us a trusted partner in the medical technology field.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Tuttlingen, Germany
- Founded
- 1994 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- frimed.de
- Categories
- Medical & Healthcare Supplies
- Markets
- Germany
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
- First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The company website was already online in 2000. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-03. Internet Archive (Wayback)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-09-17. Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- 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 2026-08-16. OpenSanctions
- 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 2026-08-16. OpenSanctions
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-18. VIES (European Commission)
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
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)
Check independently
Before a first order, ask for the ISO 13485, Medical Devices Quality certificate number, its holder and the products it covers.