Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “BIOSTER”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 370 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 363

More countries (2)

Romania 183 Czechia 180

Risk class Class I 5 Class IIa 8 Class IIb 183 Class III 174 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 Verified only

Category (EMDN)

Browse by category

370 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Traumacel TAF Light

BIOSTER, a.s.,Czechia Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumacel TAF

BIOSTER, a.s.,Czechia Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Emoxicel Taf Retilight

BIOSTER, a.s.,Czechia Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumastem NEW Dent

BIOSTER, a.s.,Czechia

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumacel FAM Strata

BIOSTER, a.s.,Czechia

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumastem TAF

BIOSTER, a.s.,Czechia Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumastem TAF Light

BIOSTER, a.s.,Czechia Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Traumastem FAM Strata

BIOSTER, a.s.,Czechia

Active Regimes: CE MDR Registry: EUDAMED Class:III

Showing 201-220 of 370

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site