FDA Device Intelligence
HomeHermann Medizintechnik GmbH › Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH

Hermann Medizintechnik GmbH · Model H-080. · UDI-DI 04059453026019

HRR
8
510(k) clearances
39
Adverse events
1
Recalls
183
Facilities

Description

VANNAS Micro Scissors, straight,3 ¼", 8cm

Recalls

DateFirmReason
2023-05-12MEDLINE INDUSTRIES, LP - NorthfieldThe scissors were manufactured without a tip protector resulting in the scissors breaking through the semi-rigid plastic tray compromising sterility.

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 docs
Data 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.