10,000 results · 93ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Accumax Lab Devices Private Limited

Manufacturer
🇮🇳 India·11 Basic UDI-DIs·11 Devices

EM DEVICE LAB, INC.

FDA registration
EM DEVICE LAB, INC.·1 product·🇺🇸 United States

ACCUMAX LAB DEVICES PVT LTD

FDA registration
ACCUMAX LAB DEVICES PVT LTD·7 products·🇮🇳 India

BreathID Hp Lab Device

FDA UDI
MERIDIAN BIOSCIENCE ISRAEL LTD·07290016923384·The BreathID® Hp Lab System is intended for use...

SALTER LABS PEP DEVICE

FDA 510(k)
FDA Class 2 ·Anesthesiology

Quickloop Abscess Treatment Device

FDA UDI
Em Device Lab, Inc·B762M01000010·Device for draining and irrigating cutaneous an...

BreathID Hp Lab Device (WIN)

FDA UDI
MERIDIAN BIOSCIENCE ISRAEL LTD·07290016923391·The BreathID® Hp Lab System is intended for use...

iFuge GC 12

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

CENTRIFUGES

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

Clinical Centrifuge

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

iFuge CYTO

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

CENTRIFUGE

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

SAMPLES ANALYSES, PLASTIC CONTAINERS - OTHER

Device
EU IVDD · Eu Ivd General ·Accumax Lab Devices Private Limited·On the market

iFuge CS2P NXT

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

iFuge D08

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

Robotic Tips

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

Robotic Tips

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

iFuge CS03 NXT

Device
EU IVDR · Eu Ivd Class A ·Accumax Lab Devices Private Limited·On the market

Lab Devices

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Champions-Implants GmbH·34 devices

SURESTEP

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code NBW·November 14, 2005