Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in MalaysiaLabelled 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 14, 2026, FDA's public records list Unomedical Sdn Bhd with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 16, 1998: EUROMEDICAL HAEMATURIA FOLEY CATHETER.
| Sep 16, 1998 | EUROMEDICAL HAEMATURIA FOLEY CATHETERK973076 · EZL | 510(k) clearances |
| Nov 21, 1996 | EUROMEDICAL REINFORCED ENDOTRACHEAL TUBEK962389 · BTR | 510(k) clearances |
| Dec 8, 1995 | PEDIATRIC WIRE REINFORCED SILICONE ENDOTRACHEAL TUBEK954750 · BTR | 510(k) clearances |
| Dec 8, 1995 | SILICONE ENDOTRACHEAL TUBEK954751 · BTR | 510(k) clearances |
| Dec 8, 1995 | PEDIATRIC SILICONE ENDOTRACHEAL TUBEK954753 · BTR | 510(k) clearances |
| Dec 8, 1995 | WIRE REINFORCED SILICONE ENDOTRACHEAL TUBEK954754 · BTR | 510(k) clearances |
| May 22, 1995 | PEDIATRIC ENDOTRACHEAL TUBEK951697 · BTR | 510(k) clearances |
| May 22, 1995 | ENDOTRACHEAL TUBEK951696 · BTR | 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
