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 00763000871178
Covidien llc
·
,
United States
Class III
CE/MDR
Active
CE MDR
EUDAMED
III
340 variants
Hernia Procedure Pack
BOX00042V6
Hernia Procedure Pack
BOX01792V1
Hernia Procedure Pack
BOX02173V5
Hernia Procedure Pack
BOX06463V1
Hernia Procedure Pack
BOX06720V2
Hernia Procedure Pack
BOX07226V1
Hernia Procedure Pack
BOX07628V2
Hernia Procedure Pack
BOX08048V1
Hernia Procedure Pack
BOX08287V1
Hernia Procedure Pack
BOX08545V1
Hernia Procedure Pack
BOX08969V1
Hernia Procedure Pack
BOX09291V2
Hernia Procedure Pack
BOX09847V1
Hernia Procedure Pack
DXT1510ARIGLA
Hernia Procedure Pack
DXT1510ARPRO
Hernia Procedure Pack
K-BE-HER108-008
See all variants of this device
Previous
Next
Showing 301-320 of 342