16 results · 18ms · Sources: EU EUDAMED, US FDA

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<GENX> DOUBLE LUMEN NEEDLE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Inrad

FDA UDI
Inrad·00817295020640·SelectCore Variable Throw Biopsy Device 20 ga x...

SCOTT'S BENT NEEDLE TIPS (100) BLACK 20 G

FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819910201·SCOTT'S BENT NEEDLE TIPS (100) BLACK 20 G

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668112267·SURG-I-BAND ORANGE

BLUEPHASE 20I

FDA 510(k)
FDA Class 2 ·Dental

G210 InviCell Plus with SignipHy pH monitoring

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 2018

ZMR®

FDA UDI
Zimmer, Inc.·00889024161986·

NexGen® Complete Knee Solution

FDA UDI
Zimmer, Inc.·00889024224445·

ZMR®

FDA UDI
Zimmer, Inc.·00889024161993·

BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018

BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018

SPINNING SPIROS CLOSED MALE LUER, RED CAP

FDA Adverse Event
Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·December 1, 2020

FLOGARD

FDA Adverse Event
Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·March 6, 2013

CRYSTALENS

FDA Adverse Event
Injury ·BAUSCH + LOMB·Product code NAA·February 11, 2011

SPRINT QUATTRO SECURE S

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·August 8, 2014