PSR - Peri-oral/orbital Photodamage & Rhytides

FDA registration

ENERGIST LIMITED·1 product·🇬🇧 United Kingdom

Shalya iLUX Surgical Light with Camera- Display system: iLUX 20-20 M/W/O/C-D

FDA registration

XCELLANCE MEDICAL TECHNOLOGIES PVT. LTD.·1 product·🇮🇳 India

Remunity

FDA UDI

United Therapeutics Corporation·00850017421073·OVER PACK, DISPOSABLE KIT, UNITY 00850017421073...

Remunity

FDA UDI

United Therapeutics Corporation·00850017421035·STARTER KIT, PHARMACY FILL, UNIT One starter ki...

Remunity

FDA UDI

United Therapeutics Corporation·00850017421097·DKPI-21128-001 SPECIALTY PHARMACY ACCESSORY KIT...

Bag, Urine Collection, Leg, For External Use, Non-Sterile

FDA classification

FDA Class 1 ·Bag, Urine Collection, Leg, For External Use, Non-Sterile

STERYLAB S.R.L.

Manufacturer

🇮🇹 Italy·1 Basic UDI-DI·1 Device·ITALCERT SRL, ITALCERT SRL, ITALCERT SRL, ITALCERT SRL, and ITALCERT SRL

Trial Implants

Basic UDI-DI

EU MDR · Eu Md Class 2a ·AQ Solutions GmbH·128 devices

Drills and Accessories

Basic UDI-DI

EU MDR · Eu Md Class 2a ·AQ Solutions GmbH·10 devices

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Venovo Venous Stent System

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·DIGENE HC2 SYSTEM SOFTWARE

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·cobas HPV Test

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·cobas HPV Test, 240 Tests, cobas HPV Test, 960 Tests

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·DIGENE HYBRID CAPTURE 2 HPV DNA TEST

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·cobas HPV Test

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Zilver Vena® Venous Self-Expanding Stent

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·BD Onclarity HPV Assay

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·HYBRID CAPTURE 2 HIGH-RISK HPV DNA TEST AND HYBRID CAPTURE HPV DNA TEST

Kit, Dna Detection, Human Papillomavirus

FDA Pre-Market Approval

FDA Class 3 ·BD Onclarity HPV Assay, BD Viper LT System