51 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HARDYDISK, STREPTOMYCIN 10MCG
FDA 510(k)
FDA Class 2
·Microbiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756236782·CERVICAL COLLAR
SILVERVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000160·SILVERVENT 2 IC, SIZE 1
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E89620002010·Needle holders 18cm straight diamond
coated...
SR Facebow
FDA UDI
ORMCO CORPORATION·00889989023121·Facebow LONG SZ 1 .044 DIA.
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481109942·Low Retention Insert, LOCATOR R-Tx Attachment S...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993130627·CUSTOM SEAMLESS SOFT 1/KNEE HIGH/OPEN TOE/SAND
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993128990·CUSTOM SEAMLESS SOFT 1/MID THIGH HIGH/OPEN TOE/...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993131754·CUSTOM SEAMLESS SOFT 1/AG-HT ONE LEG PANTY/OPEN...
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993132539·CUSTOM SEAMLESS SOFT 1/THIGH HIGH/OPEN TOE/SAND
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993125913·CUSTOM SEAMLESS SOFT 1/PANTY/OPEN TOE/SAND
JOBST Custom Seamless Soft
FDA UDI
BSN-Jobst GmbH·04059993126132·CUSTOM SEAMLESS SOFT 1/CHAP STYLE/OPEN TOE/SAND
NED-000201 CEL-MIR-40 ASSAY
FDA UDI
LIFE TECHNOLOGIES CORPORATION·10190302016315·NED-000201 CEL-MIR-40 ASSAY
LOCATOR, Dentsply Sirona System
FDA UDI
Zest Anchors, LLC·00840481131776·LOCATOR R-Tx Low Retention Insert (4 pack)
AESCULAP BONE WAX
FDA 510(k)
FDA Unclassified
·Unknown
WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEYER-SCHULTE ROUND GEL INFLATABLE, 425 CC
FDA Adverse Event
V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·December 21, 1993
MCS+9000 WITH PLASMA SET W/FILTERS, BMB
FDA Adverse Event
Malfunction
·HAEMONETICS, INC.·Product code GKT·January 12, 2022
I-FACTOR PUTTY
FDA Adverse Event
Injury
·CERAPEDICS INC.·Product code MBS·March 12, 2024
88-000201 ADULT G/PAD MONO ADHESIVE
FDA Adverse Event
Injury
·DEROYAL·Product code GEI·July 28, 2000