10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Lympha Press Pants NCR-PNT
FDA UDI
MEGO afek Agricultural Cooperative Society Ltd·07290105874122·The Lympha Press Pants NCR-PNT compression garm...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664816540·Reusable SpO2 Sensor/Nellcor/Soft finger cover/...
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007453·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007477·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007439·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007408·
Lympha Press Pants(FB) NCR-PNT
FDA UDI
MEGO afek Agricultural Cooperative Society Ltd·07290105876522·The Lympha Press Pants(FB) NCR-PNT compression ...
Lympha Press Pants(FS) NCR-PNT
FDA UDI
MEGO afek Agricultural Cooperative Society Ltd·07290105876539·The Lympha Press Pants( FS) NCR-PNT compression...
Lympha Press Pants(FS-XL)NCR-PNT
FDA UDI
MEGO afek Agricultural Cooperative Society Ltd·07290105876638·The Lympha Press Pants (FS-XL) NCR-PNT compress...
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007484·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007446·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007460·
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007415·
MaxLock Extreme™
FDA UDI
TORNIER, INC.·00846832054046·MedialMax™ NC Fusion PocketLock™ Plate
Sensoronics
FDA UDI
SENSORONICS INCORPORATED·00851456007422·
PLMA DVC V11.51 1 N CR
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 21, 2017
PLMA DVC V11.51 1 N CR
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·March 10, 2016
Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with an Argon flush. The vacuum sealed product is then placed into a Tyvek/film pouch and that pouch is heat sealed. The fully pouched product is then labeled and placed into a carton with an IFU. The carton is then labeled and shrink wrapped. The labels also include a sterilization indication dot. This system is intended for primary and revision total shoulder arthroplasty, as well as hemi-arthroplasty
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·June 7, 2017
Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with an Argon flush. The vacuum sealed product is then placed into a Tyvek/film pouch and that pouch is heat sealed. The fully pouched product is then labeled and placed into a carton with an IFU. The carton is then labeled and shrink wrapped. The labels also include a sterilization indication dot. This system is intended for primary and revision total shoulder arthroplasty, as well as hemi-arthroplasty
FDA Recall
Terminated
·Zimmer Biomet, Inc.·Product code KWS·April 26, 2017
NFLEX CURVED ROD 70MM-STERILE
FDA Adverse Event
Injury
·SYNTHES ELMIRA·Product code NQP·June 16, 2017