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Aurelia Robust

by Maxter Glove Manufacturing Sdn Bhd 5 variants

Ref L, XS, XL

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number09555002102234 UDI-DI Date8 Feb 2024ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number955500211638CT Basic UDI-DI Date8 Dec 2021RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Aurelia Robust EUDAMEDGUDID
Aurelia Robust 9.0 EUDAMED
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / Reference
L EUDAMED
XS EUDAMED
XL EUDAMED
93895 GUDID
93898 GUDID
Primary DI / UDI-DI
09555002102234, 09555002102203, 09555002102906
Basic UDI-DI
955500211638CT
FDA Product Code
LZA
EMDN Code
T01020204 Nitrile examination / treatment gloves
GMDN Term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device Class
Class I
Regulation Number
880.6250
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
L
XS
XL
GUDID
93895
93898

Manufacturer details

EUDAMED SRN
MY-MF-000016719
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Maxter Glove Manufacturing Sdn Bhd

See all devices from Maxter Glove Manufacturing Sdn Bhd →

Properties

  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Manufacturing Date

Other properties (20)

  • 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
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No