R210250 NAC Attack

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

Multiple

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES (LOMEFLOXACIN)

FDA registration

TREK DIAGNOSTIC SYSTEMS, LTD.·1 product·🇬🇧 United Kingdom

SENSITITRE SUSCEPTIBILITY PLATES (CEFOTAXIME)

FDA registration

TREK DIAGNOSTIC SYSTEMS, LTD.·1 product·🇬🇧 United Kingdom

Oxoid Mycoplasma Syupplement

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom

Susceptibility Test Discs, Antimicrobial

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom

Patient Lift Sling

FDA registration

DONGGUAN ELLIAN ENTERPRISE, LTD.·1 product·🇨🇳 China

Oxoid O.G.Y.E.SELECTIVE SUPPLEMENT

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom

R2476096 ProSpecT Campylobacter Microplate Assay 96 Tests

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom

Staphylococcus Aureus Somatic Antigens

FDA registration

OXOID, LTD.·1 product·🇬🇧 United Kingdom

LAP Disk

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

R21206 Bile Solubility Reagent (10%)

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

OXOID PYLORI TEST

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

Sterile Sling

FDA registration

DONGGUAN ELLIAN ENTERPRISE, LTD.·1 product·🇨🇳 China

FROGFISH INTERNATIONAL CORP.

FDA registration

FROGFISH INTERNATIONAL CORP.·1 product·🇹🇼 Taiwan

Lens, Contact, Orthokeratology, Overnight

FDA Pre-Market Approval

FDA Class 3 ·Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact

CSZ Reusable General Purpose Temperature Probe, 12Fr

Basic UDI-DI

EU MDD · Eu Md Class 2a ·Measurement Specialties Inc.·1 device

CSZ Reusable Skin Temperature Probe, Attached Surface

Basic UDI-DI

EU MDD · Eu Md Class 2a ·Measurement Specialties Inc.·1 device

CSZ General Purpose Temperature Probes (4491 Variant)

Basic UDI-DI

EU MDD · Eu Md Class 2a ·Measurement Specialties Inc.·1 device

PATIENT EXAMINATION GLOVES (LATEX)

FDA 510(k)

FDA Class 1 ·General Hospital