audifon

FDA UDI

audifon GmbH & Co. KG·EADF022535871331217201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF0225358713312717201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF022535871331317201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF0225358713338117201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF0225358713338217201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF022535871332517201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF0225358713315917201·BTE

audifon

FDA UDI

audifon GmbH & Co. KG·EADF0225358713312017201·BTE

3T Foot Ankle 16 pTx

FDA UDI

Siemens Shenzhen Magnetic Resonance Ltd.·04056869015491·MRI Coil

PTX GLENOID GUIDE S50/S (WOS)

FDA UDI

FOURNITURES HOSPITALIERES INDUSTRIE·03661489698958·

PTX GLENOID GUIDE S48/S (WOS)

FDA UDI

FOURNITURES HOSPITALIERES INDUSTRIE·03661489698941·

PTX GLENOID GUIDE S44/S (WOS)

FDA UDI

FOURNITURES HOSPITALIERES INDUSTRIE·03661489698927·

PTX GLENOID GUIDE S46/S (WOS)

FDA UDI

FOURNITURES HOSPITALIERES INDUSTRIE·03661489698934·

3T Foot Ankle 16 pTx Kit

FDA UDI

Siemens Shenzhen Magnetic Resonance Ltd.·04056869015507·Contains Medical Device Mat. 10837233 (GTIN:040...

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver PTX Drug-Eluting Peripheral Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·ZILVER PTX DRUG-ELUTING PERIPHERAL STENT

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver PTX Drug-Eluting Peripheral Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver PTX Drug-Eluting Peripheral Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver PTX Drug-Eluting Peripheral Stent

Stent, Superficial Femoral Artery, Drug-Eluting

FDA Pre-Market Approval

FDA Class 3 ·Zilver PTX Peripheral Drug-Eluting Stent