11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Glide-On Vinyl Examination Gloves
FDA 510(k)
FDA Class 1
·General Hospital
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100233·LIEBERMAN ASPIRATING SPECULUM V-WIRE
MaxFuse,VBR, 12 (D) x 14 (W) x 33 (H)
FDA UDI
Pioneer Surgical Technology, Inc.·00846468056285·12 (D) x 14 (W) x 33 (H)
ORTHOSCAN, ORTHOSCAN HD
FDA 510(k)
FDA Class 2
·Radiology
THERMO SCIENTIFIC CEDIA OPIATE OFT ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PASSEO-18 5/200/90
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·September 28, 2021
PASSEO-18 6/200/90
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·September 28, 2021
PASSEO-18 2.5/170/130
FDA Adverse Event
Malfunction
·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code LIT·January 20, 2021
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC, CRMD·Product code DTB·January 13, 2014
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC MILACA INC.·Product code LWP·June 7, 2013
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 6, 2011