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sempermed velvet XP (100)

by HARPS Investment Asia Pte. Ltd. 5 variants

Ref 3000015971, 3000015970, 3000015965, 3000015969Model Non sterile, single use, powder free, nitrile, examination glove, ambidextrous, violet blue

Active European Union and United States

CE MDR 510(k)

Valid until

Not listed

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K223903↗

+1 more

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number9001570N*F-035VB-N-3TY Basic UDI-DI Date10 Mar 2026RegisteredStatusActive
United StatesFDA 510(k) 510(k) NumberK223903 Date27 Jan 2023IssuedStatusActive

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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • United States FDA 510(k) Active
  • European Union CE/MDR Active

Specification

EUDAMED · 510(k)

Trade Name
sempermed velvet XP (100)
sempermed velvet (100)
Model / Reference
Non sterile, single use, powder free, nitrile, examination glove, ambidextrous, violet blue, 3000015971, 3000015970, 3000015965, 3000015969
Primary DI / UDI-DI
09001570549860, 09001570549846, 09001570549754, 09001570549839
Basic UDI-DI
9001570N*F-035VB-N-3TY, 9001570N*F-030VB-N-3RB
Unit of Use DI
09001570542144, 09001570542397, 09001570542373
EMDN Code
T01020204 Nitrile examination / treatment gloves
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
SG-MF-000001645
Authorised representative
HARPS Europe GmbH AT-AR-000040870

Other devices from HARPS Investment Asia Pte. Ltd.

See all devices from HARPS Investment Asia Pte. Ltd. →

Properties

Other properties (13)

  • Sterile: No
  • 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