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Haemolance Plus, safety lancet Normal Flow, 21G 1.8mm

by Htl Strefa S a 2 variants

Ref 7372Model Type 420

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-05907506237457 Basic UDI-DI 05907506237457UDI-DIDate5 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05907506237457 UDI-DI Date1 Jun 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  • Withdrawn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
Haemolance Plus EUDAMED
Haemolance Plus, safety lancet GUDID
Generic Name
Blood lancet, single-use
Model / Ref / Catalog
Type 420, 7372, Normal Flow, 21G 1.8mm
Description
Safety lancets are sterile, single use medical devices intended for capillary blood sampling.
Primary DI / UDI-DI
05907506237457
Basic UDI-DI
B-05907506237457
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
Czechia
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Type 420
7372
GUDID
Normal Flow, 21G 1.8mm
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