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Ti̇o Medi̇kal

by Ti̇o Medi̇kal Tibbi̇ Ürünler Turi̇zm İnşaat San. Ti̇c.ltd. Şti̇ 84 variants

Ref 571.02.R03.01

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 Number86801035TIO2H Basic UDI-DI 08680110151995UDI-DIDate7 Mar 2023RegisteredStatusActive

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  • Withdrawn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
Craniotomy Drape Set
Model / Reference
571.02.R03.01
Primary DI / UDI-DI
08680110151995
Basic UDI-DI
86801035TIO2H
Direct Marketing DI
08680110151995
EMDN Code
T020199 Surgical drapes - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019233

Other devices from Ti̇o Medi̇kal Tibbi̇ Ürünler Turi̇zm İnşaat San. Ti̇c.ltd. Şti̇

See all devices from Ti̇o Medi̇kal Tibbi̇ Ürünler Turi̇zm İnşaat San. Ti̇c.ltd. Şti̇ →

Properties

  • Sterile

Other properties (12)

  • Implantable: 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