Medical Device Catalogue

51 devices foundsorted by relevance

Single Use Guide Sheath Kit K-204

Olympus Medical Systems Corporation,FDA registration: Japan

Withdrawn Registry: GUDID Class:II
Single Use Guide Sheath Kit K-203

Olympus Medical Systems Corporation,FDA registration: Japan

Withdrawn Registry: GUDID Class:II
Single Use Guide Sheath Kit K-201

Olympus Medical Systems Corporation,FDA registration: Japan

Withdrawn Registry: GUDID Class:II
Single Use Guide Sheath Kit K-401

Olympus Medical Systems Corporation,FDA registration: Japan

None Registry: GUDID Class:II
Single Use Guide Sheath Kit K-401, K-402, & Single Use Guiding Device CC-220DR

Olympus Medical Systems Corp.,FDA registration: United States

Active Regimes: 510(k) Registry: 510(k) Class:II
Single Use Guide Sheath Kit-401, K-402

Olympus Medical Systems Corp.,FDA registration: United States

Active Regimes: 510(k) Registry: 510(k) Class:II
Single Use Guide Sheath Kit

Beijing LepuImage Technology Co., Ltd.,China

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Single Use Guide Sheath Kit

Alton (Shanghai) Medical Instruments Co., Ltd.,China

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 41-51 of 51

Results for “Single Use Guide Sheath Kit”