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Fibre light carrier
Spiggle & Theis Medizintechnik GmbH · Model 20-155-00 · UDI-DI 04250676701800
EQH
Prescription
10
510(k) clearances
36
Adverse events
1
Recalls
99
Facilities
Description
for Killian septum specula 20-155-40 20-155-55, 20-155-75, 20-155-90
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-07 | Boston Scientific Corporation | Light Degradation in transmission-A film may deposit on the front face and limit transmission of light |
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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.