10,000 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071214·CERAMO CLOWARD bone curette, size 0, back angle...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071313·CERAMO CLOWARD bone curette size 5, back angled...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071238·CERAMO CLOWARD bone curette, size 1, back angle...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071207·CERAMO CLOWARD bone curette, size 0, back angle...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071252·CERAMO CLOWARD bone curette, size 2, back angle...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071276·CERAMO CLOWARD bone curette, size 3, back angle...

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749071290·CERAMO CLOWARD bone curette size 4, back angled...

BSSO INFERIOR ALVOLAR NRV DISS

FDA UDI
W.H. Holden, Inc.·D92820071120·

CHIN OSTEO-MENTL NRV RETRACTOR

FDA UDI
W.H. Holden, Inc.·D9282007170·

BSSO INFERIOR ALVOLAR NRV DISS

FDA UDI
W.H. Holden, Inc.·D9282007110·

BSSO INFERIOR ALVOLAR NRV DISS

FDA UDI
W.H. Holden, Inc.·D92820071110·

BSSO INFERIOR ALVOLAR NRV DISS

FDA UDI
W.H. Holden, Inc.·D928200711HO0·

NRV ASSEMBLY - ASTRAL

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·January 9, 2020

NRV ASSEMBLY - ASTRAL

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·January 9, 2020

ASTRAL 150 DBL KIT FRA

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·November 8, 2022

ASTRAL 150 DBL KIT FRA

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·November 8, 2022

ASTRAL 150 - FRA

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·January 5, 2022

ASTRAL 150 - FRA

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·January 5, 2022

ASTRAL 100 - EUR1

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·May 21, 2022

ASTRAL 100 - EUR1

FDA Adverse Event
Malfunction ·RESMED LTD·Product code CBK·May 21, 2022