Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Automatic Core Biopsy Instrument”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
738
FDA 510(k) incl. De Novo
3
FDA PMA
GUDID
171
Country / market
European Union (all)
737
United States
174
More countries (5)
Germany
715
Italy
15
Spain
4
Netherlands
3
Türkiye
1
Risk class
Class I
Class IIa
738
Class IIb
Class III
Class II (US)
3
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
Verified only
Category (EMDN)
Browse by category
Apply filters
741 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Disposable Automatic Core Biopsy Instruments
Suzhou Leapmed Healthcare Corporation
·
,
China
FDA 510(k)
K212284
Active
Cleared 10 Nov 2021
CE/MDR
Active
Regimes:
CE MDR
510(k)
Registry:
EUDAMED
Class
Class:
IIa
Previous
Next
Showing 741-741 of 741