Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
1 active
Filters
1 active
Registry
EUDAMED
177
FDA 510(k)
2
FDA PMA
GUDID
33
Country / market
European Union (all)
177
United States
35
More countries (1)
Ireland
177
Risk class
Class I
1
Class IIa
Class IIb
Class III
177
Class II (US)
34
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
Reset
212 devices found
·
sorted by relevance
Key
Manufacturer: Ceramisys Ltd
×
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
IntraumaBone
UDI-DI 05060171626350
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
73 variants
IntraumaBone
INB-B051020
IntraumaBone
INB-B051240
IntraumaBone
INB-B103030
IntraumaBone
INB-G20
IntraumaBone
INB-W20201608
IntraumaBone
INB-W20251206
IntraumaBone
INB-W20251407
See all variants of this device
ReproBone
UDI-DI 05060171628071
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
73 variants
ReproBone
RB7.5D15
ReproBone
RB10D4
ReproBone
RB10D7
ReproBone
RB081520
ReproBone
RWG305
ReproBone
RWG404
ReproBone
RWG602
ReproBone
RWG603
See all variants of this device
Eliz
UDI-DI 05060171625865
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
20 variants
Eliz
4912414
See all variants of this device
Repros
UDI-DI 05060171627449
Ceramisys Ltd
·
,
United Kingdom
Class III
CE/MDR
MDR 780338
Active
Valid to May 2031
Active
CE MDR
EUDAMED
III
11 variants
See all variants of this device
Previous
Next
Showing 121-140 of 212