Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Hernia Procedure Pack”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
342
FDA 510(k)
FDA PMA
GUDID
Country / market
Risk class
Class I
Class IIa
Class IIb
Class III
342
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
342 devices found
·
sorted by relevance
Key
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Hernia Procedure Pack
UDI-DI 00199150045198
Covidien llc
·
,
United States
Class III
CE/MDR
Active
CE MDR
EUDAMED
III
340 variants
Hernia Procedure Pack
BOX02160V2
Hernia Procedure Pack
BOX08047V1
Hernia Procedure Pack
BOX08213V1
Hernia Procedure Pack
BOX08559V1
Hernia Procedure Pack
BOX08961V1
Hernia Procedure Pack
BOX09089V1
Hernia Procedure Pack
BOX09291V3
Hernia Procedure Pack
BOX09482V1
Hernia Procedure Pack
BOX09848V1
Hernia Procedure Pack
DIRHERNIA
Hernia Procedure Pack
KIT01061
Hernia Procedure Pack
KIT2928V2
Hernia Procedure Pack
KOTAPPL
Hernia Procedure Pack
LAP5511I
Hernia Procedure Pack
TAPPDXT1510AR
Hernia Procedure Pack
TAPPDXT1612AR1
See all variants of this device
Previous
Next
Showing 101-120 of 342