VERIFY SixCess 275F 3 Challenge Pack (LCC014) (HP-MF, LC-SD)

FDA registration

ALBERT BROWNE LTD.·1 product·🇬🇧 United Kingdom

VERIFY SixCess 275F 3 Challenge Pack (LCC014) (HP-MF, LC-SD)

FDA registration

STERIS Corporation·1 product·🇺🇸 United States

VERIFY CHALLENGE PACKS - VERSION 2

FDA 510(k)

FDA Class 2 ·General Hospital

BiTrac

FDA registration

Pulmodyne Inc.·1 product·🇺🇸 United States

Abbott Vascular

FDA registration

CENTERPIECE S. DE R.L DE C.V (sterilization site)·1 product·🇲🇽 Mexico

IIMED MEDICAL MEXICANA S. DE R.L. DE C.V.

FDA registration

IIMED MEDICAL MEXICANA S. DE R.L. DE C.V.·1 product·🇲🇽 Mexico

Indicator, Physical/Chemical Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Physical/Chemical Sterilization Process

Stellartech Research Corp.

FDA registration

Stellartech Research Corp.·1 product·🇺🇸 United States

Atlantis 018 40 MHz Peripheral Imaging Catheter

FDA registration

Sterigenics US LLC·2 products·🇺🇸 United States

5290-011-000;5290-340-000;5290-530-000;5290-540-000;5290-628-000;5290-635-000;5290-638-000;5290-645-000

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

AVANTE CURELIGHT

FDA 510(k)

FDA Class 2 ·Dental

MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polypropylene

Activator, Ultraviolet, For Polymerization

FDA classification

FDA Class 2 ·Activator, Ultraviolet, For Polymerization