FAICO CMF System

FDA UDI

FAICO MEDICAL LLC·00840192714404·Mandibular Screw. CROSS HEAD. D.2.7x16mm - Self...

FAICO CMF System

FDA UDI

FAICO MEDICAL LLC·00840192714442·Mandibular Screw. EMERGENCY. CROSS HEAD. D.3.0x...

FAICO CMF System

FDA UDI

FAICO MEDICAL LLC·00840192714435·Mandibular Screw. EMERGENCY. CROSS HEAD. D.3.0x...

FAICO CMF System

FDA UDI

FAICO MEDICAL LLC·00840192714398·Mandibular Screw. CROSS HEAD. D.2.7x14mm - Self...

TRI

FDA UDI

TRI Dental Implants Int. AG·07640149886948·

TRI

FDA UDI

TRI Dental Implants Int. AG·07640149886931·

TOMTAR MR-S SB 51, Mangan Grey Metallic, Trommelbremse u. doppelte Kreuzstrebe

Device

EU MDR · Eu Md Class 1 ·DIETZ GmbH·On the market

TOMTAR MR-S SB 48, Mangan Grey Metallic, Trommelbremse u. doppelte Kreuzstrebe

Device

EU MDR · Eu Md Class 1 ·DIETZ GmbH·On the market

TOMTAR MR-S

Basic UDI-DI

EU MDR · Eu Md Class 1 ·DIETZ GmbH·10 devices

BULION MRS FARA GLUCOZA 500gr

Basic UDI-DI

EU IVDR · Eu Ivd Class A ·SC MEDICAMED MARKET SRL·1 device

N/A

FDA UDI

HARDY DIAGNOSTICS·00816576026173·Mannitol Salt Agar (MSA) with Oxacillin, 15x100...

IMAGE DIAGNOSTICS, INC

FDA UDI

IMAGE DIAGNOSTICS, INC.·00850977007966·IDI,RADIATION SHIELD SYSTEM,PROTEGO,MOBILE,METR...

IMAGE DIAGNOSTICS, INC

FDA UDI

IMAGE DIAGNOSTICS, INC.·00850977007782·IDI,RADIATION SHIELD SYSTEM,PROTEGO,MOBILE,METR...

IMAGE DIAGNOSTICS, INC

FDA UDI

IMAGE DIAGNOSTICS, INC.·00850977007973·IDI,RADIATION SHIELD SYSTEM,PROTEGO,MOBILE,METR...

IMAGE DIAGNOSTICS, INC

FDA UDI

IMAGE DIAGNOSTICS, INC.·00850977007652·IDI,RADIATION SHIELD SYSTEM,PROTEGO,MOBILE,METR...

Prism View

FDA UDI

PRISM CLINICAL IMAGING, INC.·B358PCI01PV0·Prism View provides both analysis and viewing c...

Prism View

FDA UDI

PRISM CLINICAL IMAGING, INC.·B358PCI01PV410·Prism View provides both analysis and viewing c...

Test System, Nicotine, Cotinine, Metabolites

FDA classification

FDA Class 1 ·Test System, Nicotine, Cotinine, Metabolites

R01483 HE Agar (Hektoen Enteric)

FDA registration

REMEL, INC.·1 product·🇺🇸 United States

R01483 HE Agar (Hektoen Enteric)

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom