Home › Technomed Engineering B.V. › Neurosign

Neurosign

Technomed Engineering B.V. · Model NM-Kit 1 · UDI-DI 08720791371463

GXZ IKT Prescription

510(k) clearances

329

Adverse events

Recalls

Facilities

Description

NM-Kit 1 contains the following devices: 1x 3601-00-TE, UDI pouch: 08718375864982 2x 1699-00-TE, UDI pouch: 08718375865224 1x 1705-00-TE, UDI pouch: 08718375865231

Recalls

Date	Firm	Reason
2021-12-08	Technomed Europe	There is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01	Stryker Instruments Div. of Stryker Corporation	Defects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.

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 key Read 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.