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212 devices found
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Manufacturer: Ceramisys Ltd
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Device · Manufacturer · Authorizations
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ReproBone
UDI-DI 05060171627814
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
73 variants
ReproBone
RB20D5
ReproBone
RB124
ReproBone
RWG203
ReproBone
RWG504
See all variants of this device
IntraumaBone
UDI-DI 05060171626251
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
73 variants
IntraumaBone
INB-B051040
IntraumaBone
INB-B081520
IntraumaBone
INB-B101040
IntraumaBone
INB-C5D10
IntraumaBone
INB-C10D6
IntraumaBone
INB-W20250603
IntraumaBone
INB-W30351005
See all variants of this device
Eliz
UDI-DI 05060171625834
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
20 variants
Eliz
4911150
Eliz
4912410
Eliz
4912480
See all variants of this device
ReproBone RBD2.5
Ceramisys Ltd
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
Orbtex Orbital Implant RPX18
Ceramisys Ltd
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
ReproBone RBD5
Ceramisys Ltd
·
,
FDA registration: United Kingdom
Class II
GUDID
not on market
Withdrawn
GUDID
II
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Showing 161-180 of 212