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Rubber Polishers

by Kerr Italia SRL 65 variants

Ref ID 4110 B, 487056, 101S4W2, 8003 B, 101KW2, 100G6W2, ID 5711 B, PROP4, ID 5031/12, ID 5691 B, ID 5061/12, 101L4W2, PRX9, 101C8W2, 101AW2, 2652, 101H13W2, ID 5041 RA, 101C6W2, PRP7, ID 5491 B, 950, 882360, 101A9W2, 8002, ID 5091 B, ID 4051 B, ID 5011 B, ID 5611 B, ID 4541 B, 2653 B, 2654, ID 5091/12, 2651, ID 4041 B, 2664 B, ID 5481 RA, 100B8W2, ID 5501/8, PROP11, ID 5721/6, ID 5471 RA, 100G9W2, 101F4W2, ID 4041/12, 101L8W2, 2654 B, 100B6W2, ID 5081 B, PRP, 101A7W2

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805151187100011152 Basic UDI-DI Date25 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
ID 4110 B, 487056, 101S4W2, 8003 B, 101KW2, 100G6W2, ID 5711 B, PROP4, ID 5031/12, ID 5691 B, ID 5061/12, 101L4W2, PRX9, 101C8W2, 101AW2, 2652, 101H13W2, ID 5041 RA, 101C6W2, PRP7, ID 5491 B, 950, 882360, 101A9W2, 8002, ID 5091 B, ID 4051 B, ID 5011 B, ID 5611 B, ID 4541 B, 2653 B, 2654, ID 5091/12, 2651, ID 4041 B, 2664 B, ID 5481 RA, 100B8W2, ID 5501/8, PROP11, ID 5721/6, ID 5471 RA, 100G9W2, 101F4W2, ID 4041/12, 101L8W2, 2654 B, 100B6W2, ID 5081 B, PRP, 101A7W2
Primary DI / UDI-DI
08055165080154, 08055165079424, 08055165080901, 08055165079936, 08055165080512, 08055165080574, 08055165080383, 08055165081083, 08055165079714, 08055165080376, 08055165079721, 08055165080864, 08055165080970, 08055165080703, 08055165080796, 08055165079356, 08055165080529, 08055165080246, 08055165080680, 08055165081021, 08055165080338, 08055165079639, 08055165079592, 08055165080789, 08055165079547, 08055165080277, 08055165080130, 08055165080222, 08055165080345, 08055165080185, 08055165079851, 08055165079363, 08055165079752, 08055165035277, 08055165080123, 08055165079905, 08055165080321, 08055165080642, 08055165079806, 08055165081076, 08055165079813, 08055165080314, 08055165080604, 08055165080437, 08055165079677, 08055165080871, 08055165079868, 08055165080628, 08055165080260, 08055165081069, 08055165080765
Basic UDI-DI
805151187100011152
Unit of Use DI
08055165078793, 08055165078922, 08055165078847
EMDN Code
Q01010403 Dental abrasive and polishing materials
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007768

Other devices from Kerr Italia SRL

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Properties

  • Implantable

Other properties (12)

  • Sterile: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No