Solution Set for Epidural Use

FDA registration

BAXTER HEALTHCARE CORPORATION·1 product·🇺🇸 United States

Solution Set for Epidural Use

FDA registration

Baxter Healthcare, S.A.·1 product·🇩🇴 Dominican Republic

Solution Set for Epidural Use

FDA registration

Baxter Limited·1 product·🇲🇹 Malta

Solution Set for Epidural Use

FDA 510(k)

FDA Class 2 ·General Hospital

SINUSCOPE

FDA registration

ECLERIS SRL·1 product·🇦🇷 Argentina

SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPL

FDA registration

Synthes (USA) Products LLC·1 product·🇺🇸 United States

SN101 SINUSCOPE

FDA registration

EUSA GLOBAL LLC·1 product·🇺🇸 United States

AM/AT PI MDL 1-L: 4.5FR X 15CM

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Prontosan Wound Irrigation Solution 40ml

FDA registration

Rommelag CDMO GmbH·1 product·🇩🇪 Germany

Cantab Mobile

FDA registration

CAMBRIDGE COGNITION LTD.·1 product·🇬🇧 United Kingdom

MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

FDA classification

FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Set, Administration, Intravascular

FDA classification

FDA Class 2 ·Set, Administration, Intravascular

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form