Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Mulltupfer”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
127
FDA 510(k)
FDA PMA
GUDID
Country / market
European Union (all)
126
More countries (1)
Germany
126
Risk class
Class I
117
Class IIa
10
Class IIb
Class III
Class II (US)
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Validated only
Category (EMDN)
Browse by category
Apply filters
127 devices found
·
sorted by relevance
Key
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Mulltupfer
UDI-DI 110862730777
KERMA Verbandstoff GmbH
·
,
Germany
Class I
CE/MDR
Active
CE MDR
EUDAMED
I
19 variants
Mulltupfer
42511
Mulltupfer
42512
Mulltupfer
42514
Mulltupfer
42523
Mulltupfer
42524
Mulltupfer
42525
Mulltupfer
42526
Mulltupfer
42528
Mulltupfer
42530
Mulltupfer
42531
Mulltupfer
42532
Mulltupfer
42534
Mulltupfer
42535
Mulltupfer
42536
See all variants of this device
Temedia Mulltupfer, unsteril
UDI-DI 04015811138138
Holthaus Medical GmbH & Co. KG
·
,
Germany
Class I
CE/MDR
Active
CE MDR
EUDAMED
I
7 variants
Temedia Mulltupfer, unsteril
13821
Temedia Mulltupfer, unsteril
13822
Temedia Mulltupfer, unsteril
13824
See all variants of this device
BONA Mulltupfer 9 K walnuss
Wilhelm Weisweiler GmbH & Co. KG
·
,
Germany
Class I
CE/MDR
Active
CE MDR
EUDAMED
I
Previous
Next
Showing 1-20 of 127