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Razormed

by Razormed Inc. 75 variants

Ref 02840

Expiring European Union

CE MDR

Valid until

14 Jul 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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 Number28620239980 Date6 Mar 2026IssuedStatusExpiring expires 14 Jul 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Surgical Blades
Model / Reference
02840
Primary DI / UDI-DI
18903376028403
Basic UDI-DI
8903376SBWT
Unit of Use DI
08903376028406
EMDN Code
V010301 Blades with safety systems, single-use - not included in other classes
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IN-MF-000012812
Authorised representative
Advena Limited MT-AR-000000234

Related devices

Category: Manual scalpel blade, single-use

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  • Diamantine

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See all devices from Razormed Inc. →

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