Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FinlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of General ElectricLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Datex Division Instrumentarium with 55 510(k) clearances. The most recent is a 510(k) clearance dated Feb 6, 1997: AS/3 ESTPR MODULE.
| Feb 6, 1997 | AS/3 ESTPR MODULEK953175 · MLD | 510(k) clearances |
| Oct 23, 1996 | AS/3 LIGHT MONITORK961247 · DPS | 510(k) clearances |
| Feb 14, 1995 | AS/3 AIRWAY MODULEK943458 · CBS | 510(k) clearances |
| Jan 27, 1995 | AS/3 MEMORY MODULE, M0MEMK945234 · BSZ | 510(k) clearances |
| Dec 30, 1994 | DATEX AS/3 PATIENT MONITORK933156 · DPS | 510(k) clearances |
| Nov 14, 1994 | DATEX AS/3 TM ANAESTHESIA MONITORK933285 · BSZ | 510(k) clearances |
| Oct 17, 1994 | AS/3 NELLCOR COMPATIBLE SATURATION MOODULE, M-NSATK943456 · DQA | 510(k) clearances |
| Aug 9, 1994 | ANAESTHESIA RECORD KEEPERK923172 · BSZ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
