Home › Hermann Medizintechnik GmbH › Hermann Medizintechnik GmbH
Hermann Medizintechnik GmbH
Hermann Medizintechnik GmbH · Model H50-080-207 · UDI-DI 04059453057327
HFB
Prescription
10
510(k) clearances
60
Adverse events
1
Recalls
164
Facilities
Description
Uretero-Renoscope biopsy forceps,double action jaws, flexible, 5Charr., length 60cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.