24 results · 23ms · Sources: EU EUDAMED, US FDA

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System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·FLOW MIC SYSTEM

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·3M BRAND MICROBIAL PROFILE SYSTEM

NA

FDA UDI
SYNTHES (U.S.A.) LP·10705034782041·TI ANTERIOR CERVICAL COMPRESSION PL 4 LEVEL/88MM

IMPLANET SPINE SYSTEM

FDA UDI
IMPLANET·03607503505383·Straight Union Rod

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515136632·Tessier Osteotome, Straight 10mm wide 8"

NAR Kit

FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209108626·KIT, RAPID ACCESS TRAUMA SYSTEM - CUSTOM; This ...

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00812171029168·PESSARY, RING #4, W/O SUPPORT, 2.75"

ORION

FDA UDI
HNM TOTAL RECON LLC·00841742119526·ORION ø6.5mm Headless Cannulated Screw, Short T...

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 29, 2008

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 29, 2008

DELTAFILL18 6MM X 25CM

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·March 17, 2020

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

FDA Pre-Market Approval
FDA Class 2 ·SENSITITRE

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·November 16, 1999

AUTO SUTURE ENDO CLIP 5MM

FDA Adverse Event
Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·February 20, 1998

HOMECHOICE AUTOMATED PD SET W/CASSETTE 8-PRONG

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FKX·August 28, 2001