Browse medical devices in the “Surgical sutures scissors, reusable” EMDN category registered in EUDAMED. Each result links to its manufacturer, certificates, and identifiers.
363 medical devices in EUDAMED
Reusable surgical instruments › Sharp instruments, reusable › Surgical scissors, reusable
This is a sub-category of Reusable surgical instruments in the EMDN nomenclature.
Browse all Reusable surgical instruments02-236-15Risk category
Class IB-+G198022361508Organization name
Durable Hospital Supplies
F4-232Risk category
Class I++G742GENOPRSCISSORSY4Organization name
Fairmount Industries Pvt Ltd
11-830-14-07Risk category
Class I405760535NKOrganization name
KLS Martin SE & Co. KG
11-824-10-07Risk category
Class I405760535NKOrganization name
KLS Martin SE & Co. KG
11-914-20-07Risk category
Class I405760535NKOrganization name
KLS Martin SE & Co. KG
ZA-004-366Risk category
Class I40492030000047BPOrganization name
STEMA Medizintechnik GmbH
ZA-001-751Risk category
Class I40492030000047BPOrganization name
STEMA Medizintechnik GmbH
3528Risk category
Class I805660060MEDFT01IMXFOrganization name
MEDESY srl
103-077-4Risk category
Class I4251891MICROSCISSORS4FOrganization name
AR Instrumed
N13-350Risk category
Class I++G222SCISSORSASOrganization name
Euromed Industries
11-915-17-07Risk category
Class I405760535NKOrganization name
KLS Martin SE & Co. KG
PH70697Risk category
Class I0724995NHRSICUTTINGHLOrganization name
STERIS IMS Limited
PH70206Risk category
Class I0724995NHRSICUTTINGHLOrganization name
STERIS IMS Limited
124-008Risk category
Class I404911315301R002001001X3Organization name
ELCON Medical Instruments GmbH
08-8011-18Risk category
Class I4250485300000127ZEOrganization name
Zepf Medical Instruments GmbH
103-069-6Risk category
Class I4251891SCISSORSD8Organization name
AR Instrumed
PI125003Risk category
Class I++G796PI125003MROrganization name
Promed Instruments
103-123Risk category
Class I4251891SCISSORSD8Organization name
AR Instrumed
176814FXRisk category
Class IB-04250407719081Organization name
FENTEX medical GmbH
AC 509/12Risk category
Class I404953800000013AROrganization name
nopa instruments Medizintechnik GmbH
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →