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Lasec® Safety Lancets, 21G Blue Retractable Needle, pack of 200

by Lasec International (Pty) Ltd

Ref HLASLANCETBLU-21G2

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 Number600971013LANCETBLU-21G2YS Basic UDI-DI 06009710130513UDI-DIDate24 Aug 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
SAFETY LANCET, 21G NEEDLE pack of 200
Model / Reference
HLASLANCETBLU-21G2
Primary DI / UDI-DI
06009710130513
Basic UDI-DI
600971013LANCETBLU-21G2YS
EMDN Code
V010401 Lancets with safety systems, single-use
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
ZA-MF-000040804
Authorised representative
TNMC Devices Llc HR-AR-000019582

Other devices from Lasec International (Pty) Ltd

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