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Dermagrip Nitrile Ultra Lt

by WRP Asia Pacific Sdn. Bhd. 5 variants

Ref D1504-20, D1500-17, D1500-18, D1502-82, D1503-82, D1504-17, D1100-23, D1504-18, D1501-17, D1102-23, D1501-20, D1501-82, D1104-23, D1502-17, D1501-18, D1504-82, D1103-23

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number9557795NBR-EG01BE Basic UDI-DI Date15 Nov 2023RegisteredStatusActive

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  • Withdrawn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

Trade Name
Dermagrip Nitrile Ultra Lt
Dermagrip Nitrile
Dermagrip Nitrile Ultra
Device Name
Nitrile Examination Glove Powder Free, Non-Sterile
Nitrile Examination Gloves, Powder Free, Sterile
Model / Reference
D1504-20, D1500-17, D1500-18, D1502-82, D1503-82, D1504-17, D1100-23, D1504-18, D1501-17, D1102-23, D1501-20, D1501-82, D1104-23, D1502-17, D1501-18, D1504-82, D1103-23
Primary DI / UDI-DI
19557795001661, 19557795001425, 19557795001524, 09557795003941, 09557795003958, 19557795001463, 19557795001722, 19557795001562, 19557795001432, 19557795001746, 19557795001630, 09557795003934, 19557795001760, 19557795001449, 19557795001531, 09557795003965, 19557795001753
Basic UDI-DI
9557795NBR-EG01BE, 9557795NBR-EG02BG
EMDN Code
T01020204 Nitrile examination / treatment gloves
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
MY-MF-000004690
Authorised representative
REMESCO HANDELSGESMBH AT-AR-000002669

Other devices from WRP Asia Pacific Sdn. Bhd.

See all devices from WRP Asia Pacific Sdn. Bhd. →

Properties

  • Sterile NoEUDAMEDYesEUDAMED

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