6,183 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LINER 10 HOODED NEU, MP6, HXE-PLUS, 32MM
FDA Adverse Event
Injury
·Product code OQH·May 13, 2021
RESTORIS ACETABULAR LINER
FDA Adverse Event
Injury
·PIPELINE ORTHOPEDICS LLC·Product code OQH·March 25, 2013
RESTORIS ACETABULAR LINER
FDA Adverse Event
Injury
·PIPELINE ORTHOPEDICS LLC·Product code OQH·April 26, 2013
LINER/NON-HOODED-NEU, MP8, HXE-PLUS, 36MM
FDA Adverse Event
Injury
·Product code OQH·November 8, 2020
FMP HIP
FDA Adverse Event
Injury
·ENCORE MEDICAL, L.P.·Product code OQH·March 29, 2016
RESTORIS TOTAL HIP SYSTEM
FDA Adverse Event
Injury
·PIPELINE ORTHOPEDICS LLC·Product code OQH·July 18, 2013
RESTORIS ACETABULAR LINER
FDA Adverse Event
Injury
·PIPELINE ORTHOPEDICS LLC·Product code OQH·July 12, 2013
X-ALT HIP
FDA Adverse Event
Injury
·ENCORE MEDICAL L.P.·Product code OQH·October 16, 2019
Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented
FDA classification
FDA Class 2
·Hip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented
Neobiotech Implant System
FDA UDI
Neobiotech. co., ltd·08809276763082·Ø2.0-3.0, L:30.0cm
OCHS LABS, LLC
FDA registration
OCHS LABS, LLC·2 products·🇺🇸 United States
LENS
FDA UDI
Ochs Labs LLC·G253LW30·NKPW Psychophysiological biofeedback system A c...
Regenesis 3
FDA UDI
Ochs Labs LLC·G253R30·red/infrared light phototherapy unit
RENPHO Pulse Oximeter
FDA UDI
JOICOM CORPORATION·00850023727008·
RAKA OCH BOSDA PEANGER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
IMMUNO. IDENTIFICATION OF H. CAPSULATUM
FDA 510(k)
FDA Class 2
·Microbiology
HU-FRIEDY
FDA UDI
HU-FRIEDY MFG. CO., LLC·10889950045180·TG Chisel, Modified, Smooth HDL
OCH-METHVIN "HAIL STATE"
FDA UDI
APPLIED MEDICAL RESOURCES CORPORATION·30607915135158·Kit Contains:
CD001, 10mm RETRIEVAL SYSTEM, 10...
Ochs Labs EEG Amplifier
FDA UDI
SOUTHEAST SIGNAL, INC·B58802L0·EEG Amplifier
OxyMulti-Mask™
FDA UDI
Southmedic Incorporated·10620974003585·OxyMulti-Mask™ Adult with Dual Standard Connector