Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Hernia Procedure Pack”

Name, manufacturer or identifier

Manufacturer (optional)

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

342 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Hernia Procedure Pack UDI-DI 00824846019695

Covidien llc,United States Class III

Active CE MDR EUDAMED III
340 variants
- Hernia Procedure Pack BOX00042V5
- Hernia Procedure Pack BOX04363V1
- Hernia Procedure Pack BOX07628V1
- Hernia Procedure Pack BOX07673V1
- Hernia Procedure Pack BOX07679V1
- Hernia Procedure Pack BOX08965V1
- Hernia Procedure Pack BOX09091V1
- Hernia Procedure Pack BOX09095V1
- Hernia Procedure Pack BOX09841V1
- Hernia Procedure Pack BOX021222V2
- Hernia Procedure Pack ESQHERNIA
- Hernia Procedure Pack HERNIASU1612AR
- Hernia Procedure Pack LAPBIHAS
- Hernia Procedure Pack LAPUIHLH
- Hernia Procedure Pack TAPPDXT1610ALL
- Hernia Procedure Pack TEMVLOCMB5STF2
- See all variants of this device

Previous Next

Showing 1-20 of 342

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site