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 00643169855052
Covidien llc
·
,
United States
Class III
CE/MDR
Active
CE MDR
EUDAMED
III
340 variants
See all variants of this device
STM Hernia Kits Procedure Pack
Covidien llc
·
,
United States
Class III
CE/MDR
Active
CE MDR
EUDAMED
III
Previous
Next
Showing 341-342 of 342