Flotec

FDA UDI

FLOTEC INC·B741RW0·

Flotec

FDA UDI

FLOTEC INC·B741DL0·

Flotec

FDA UDI

FLOTEC INC·B741MC0·

Flotec

FDA UDI

FLOTEC INC·B741FM0·

XIANTAO FUSHI PROTECTIVE PRODUCTS CO., LTD

Manufacturer

🇨🇳 China·39 Basic UDI-DIs·39 Devices·TÜV Rheinland LGA Products GmbH and TÜV Rheinland LGA Products GmbH

Reliance Medical (Shanghai) Limited

Manufacturer

🇨🇳 China·6 Basic UDI-DIs·124 Devices·1 Importer·TÜV Rheinland LGA Products GmbH and TÜV Rheinland LGA Products GmbH

Changzhou Hualian Health Dressing Co., Ltd.

Manufacturer

🇨🇳 China·9 Basic UDI-DIs·77 Devices·3 Importers·SGS Belgium NV and TÜV SÜD Product Service GmbH

K-Pack II Needle 27 GA x 0.75" T.W. (0,4 x 20mm)

FDA UDI

MERZ NORTH AMERICA, INC.·M2139022M1X205·

AccuPort Multi Directional Delivery Canula 8 Ga x 200 mm Drill Length

FDA UDI

ZIMMER KNEE CREATIONS, INC.·00889024205215·

CFM Technologies

FDA UDI

C F M TECHNOLOGIES INC·00850013958115·Cerumen Management Set with single-use curettes.

CFM TEechnologies

FDA UDI

C F M TECHNOLOGIES INC·00850013958108·Cerumen Management Set with single-use curettes.

CFM Technologies

FDA UDI

C F M TECHNOLOGIES INC·00850013958078·Cerumen Management Set with reusable curettes. ...

CFM Technologies

FDA UDI

C F M TECHNOLOGIES INC·00850013958061·Cerumen Management Set with reusable curettes.

Pocket Ultrasound System (C10)

FDA 510(k)

FDA Class 2 ·Radiology

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·PULSAR/PULSAR MAX IMPLANTABLE PULSE GENERATOR SYSTEM WITH CONSULT SOFTWARE

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·PULSAR/PULSAR MAX IMPLANTABLE PULSE GENERATOR SYSTEM WITH CONSULT SOFTWARE

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Pulsar/Pulsar Max Implantable Pulse Generator System with Consult Software

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Pulsar/Pulsar Max Implantable Pulse Generator System with Consult Software

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval

FDA Class 3 ·FREEZOR/FREEZOR XTRA/FREEZOR MAX CRYOABLATION CATHETERS AND THE CRYOCONSOLE

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

FDA Pre-Market Approval

FDA Class 3 ·Arctic Front, Front Advance Cardiac Cryoablation, Freezor MAX & CryoConsoleSystem