Angelcup - Pink

FDA UDI

Grupo IX Kaan, S.A. de C.V.·G391ANGPKLG2·Reusable Menstrual Cup - Large Size

Angelcup - Lilac

FDA UDI

Grupo IX Kaan, S.A. de C.V.·G391ANGLILSM2·Reusable Menstrual Cup - Small Size

Angelcup - Crystal

FDA UDI

Grupo IX Kaan, S.A. de C.V.·G391ANGCRSM2·Reusable Menstrual Cup - Small Size

Angelcup - Pink

FDA UDI

Grupo IX Kaan, S.A. de C.V.·G391ANGPKSM2·Reusable Menstrual Cup - Small Size

FREEVIEW INDUSTRIAL (VIETNAM) CO., LTD

FDA registration

FREEVIEW INDUSTRIAL (VIETNAM) CO., LTD·1 product·🇻🇳 Vietnam

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

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, OVATION IX ILIAC STENT GRAFT

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

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

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room

CAREMIBRAIN

FDA 510(k)

FDA Class 2 ·Radiology

Polychloroprene Powder Free Sterile Surgical Gloves, White, Tested for Use with Chemotherapy

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

KIT,REINF 1/4"ID X 10'LG-SCAV

FDA UDI

PARKER-HANNIFIN CORPORATION·00816711022589·KIT,REINF 1/4"ID X 10'LG-SCAV

ILUMARK GmbH

Authorized representative

🇩🇪 Germany·2 Manufacturers·1 Device

CLEAR SILICONE TUBING - BY FOOT .250 ID X .500 OD

FDA UDI

W.H. Holden, Inc.·D9288330040·

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·TRIVASCULAR, INC OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, TRIVASCULAR, INC OVATION IX ILIAC STENT GRAFT

Urocare® Tubing White-Rubber with Connector 0.31" ID x 18"

FDA UDI

UROCARE PRODUCTS, INC.·00792293060167·TUBING, URINE COLLECTION, OSTOMY, WHITE-RUBBER,...

System, Endovascular Graft, Aortic Aneurysm Treatment

FDA Pre-Market Approval

FDA Class 3 ·OVATION ABDOMINAL STENT GRAFT SYSTEM, OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, OVATION IX ILIAC STENT GRAFT