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Hi-Cut

by Kehr Surgical Private Limited 14 variants

Ref 20110Model Surgical Blade No. 10

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08902283201100 Basic UDI-DI 08902283201100UDI-DIDate30 May 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Carbon Steel Surgical Blade
Model / Reference
Surgical Blade No. 10, 20110
Primary DI / UDI-DI
08902283201100
Basic UDI-DI
B-08902283201100
EMDN Code
V010302 Blades without safety systems, single-use - not included in other classes
Device Class
Class IIa
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
IN-MF-000021433
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Kehr Surgical Private Limited

See all devices from Kehr Surgical Private Limited →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No