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Surgical Guide IS Fixture Adapter_Screw

by Neobiotech Co., Ltd. 2 variants

Ref SGISFAS30

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880927676NBRSIRSCL1S03FT Basic UDI-DI 08809876905776UDI-DIDate17 Jul 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
Dental Surgical Instrument
Model / Reference
SGISFAS30
Primary DI / UDI-DI
08809876905776
Basic UDI-DI
880927676NBRSIRSCL1S03FT
EMDN Code
P01020180 Dental implants - accessories
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
KR-MF-000016946
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Neobiotech Co., Ltd.

See all devices from Neobiotech Co., Ltd. →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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