Home › AESCULAP, INC. › AESCULAP
AESCULAP
AESCULAP, INC. · Model MA351R · UDI-DI 04046964586507
HNM
Prescription
2
510(k) clearances
11
Adverse events
2
Recalls
80
Facilities
Description
BARRAQUER Micro Needle Holder, straight, 5 1/4", (134 mm), round knurled handle, with ratchet, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-11-20 | Becton Dickinson and Company | No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow. |
| 2007-11-20 | Becton Dickinson and Company | No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow |
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.