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
21
FDA 510(k)
FDA PMA
GUDID
4
Country / market
European Union (all)
21
United States
4
More countries (1)
Poland
21
Risk class
Class I
25
Class IIa
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
Reset
25 devices found
·
sorted by relevance
Key
Manufacturer: Aesculap Chifa Sp. z o.o.
×
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Chifa
UDI-DI 05906728278040
Aesculap Chifa Sp. z o.o.
·
,
Poland
Class I
CE/MDR
Active
CE MDR
EUDAMED
I
21 variants
Chifa
IM-043-140-PMK
Chifa
IM-543-002-PMK
Chifa
KO-001-002-PHMK
See all variants of this device
Aesculap MD651
Aesculap Chifa Sp Z O O
·
,
FDA registration: United States
Class I
GUDID
on market
None
GUDID
I
Previous
Next
Showing 21-25 of 25