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Medlance Plus, safety lancet Special, blade 0.8 mm 2.0 mm

by Htl Strefa S a 2 variants

Ref 7046Model type 553-556

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05907506237136 Basic UDI-DI 05907506237136UDI-DIDate8 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05907506237136 UDI-DI Date20 Feb 2020ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Medlance Plus EUDAMED
Medlance Plus, safety lancet GUDID
Generic Name
Blood lancet, single-use
Model / Ref / Catalog
type 553-556, 7046, Special, blade 0.8 mm 2.0 mm
Primary DI / UDI-DI
05907506237136
Basic UDI-DI
B-05907506237136
FDA Product Code
FMK
EMDN Code
V010401 Lancets with safety systems, single-use
GMDN Term
Blood lancet, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
878.4850
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
type 553-556
7046
GUDID
Special, blade 0.8 mm 2.0 mm
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Htl Strefa S a

See all devices from Htl Strefa S a →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (17)

  • 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No