Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025446·COPPER NITI 27 BAF 14 DIA U/S PK10

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059510·210-1064, Blue ID Tag, BAF 90 2mm SH

Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025507·COPPER NITI 27 BAF 16 DIA L/S PK10

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059312·210-1041, Blue ID Tag, BAF 0 1mm MD

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059497·210-1062, Blue ID Tag, BAF 60 2mm MD

Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025521·COPPER NITI 27 BAF 18 DIA U/S PK10

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059404·210-1053, Blue ID Tag, BAF 60 1mm MD

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059466·210-1059, Blue ID Tag, BAF 30 2mm MD

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059305·210-1040, Blue ID Tag, BAF 0 1mm SH

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059459·210-1058, Blue ID Tag, BAF 30 2mm SH

Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025460·COPPER NITI 27 BAF 14 DIA L/S PK10

Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025545·COPPER NITI 27 BAF 18 DIA L/S PK10

OsteoMed

FDA UDI

OSTEOMED LLC·00845694059411·210-1054, Blue ID Tag, BAF 60 1mm LG

Copper Ni-Ti - Archwire

FDA UDI

ORMCO CORPORATION·00889989025514·COPPER NITI 27 BAF 16 DIA L/L PK10

GSR/TEMP 2X B.F. System

FDA UDI

Technologie de Pensée Ltée·07540191000456·

BRF for cobas 8100

Device

EU IVDR · Eu Ivd Class A ·Hitachi High-Tech Corporation·On the market

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval

FDA Class 3 ·CADENCE FAMILY OF ICDS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval

FDA Class 3 ·SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·EPIC HF/ATLAS+HF FAMILY OF CRT-DS

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval

FDA Class 3 ·FRONTIER/FRONTIER II FAMILY OF CRT-PS