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Injection Acetate Frames

by Everife International Limited 73 variants

Ref MNG2829 90, MNGI0033 VER, MNGI0010 AMA, MNG2839 30, MNGI0031 NEG, MNGI0028 MAR, MNG2839 18, MNGI0027 BUR, MNGI0011 AMA, MNGI0011 MAR, MNGI0015 ROS, MNGI0028 NEG, MNGI0009 NEG, MNGI0015 NEG, MNG2829 30, MNGI0033 NEG, MNGI0032 MAR, MNGI0033 MAR, MNGI0001 AZL, MNGI0001 NEG, MNGI0010 CAR, MNG2823 60, MNGI0015 AZL, MNGI0010 AZL, MNG2839 10, MNGI0032 NEG, MNGI0010 NEG, MNGI0001 CAR, MNGI0009 AZL, MNG2838 50, MNGI0027 VER, MNGI0031 AZL

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, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number48952453FRMPX6 Basic UDI-DI Date29 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Plastic Full Rim
Model / Reference
MNG2829 90, MNGI0033 VER, MNGI0010 AMA, MNG2839 30, MNGI0031 NEG, MNGI0028 MAR, MNG2839 18, MNGI0027 BUR, MNGI0011 AMA, MNGI0011 MAR, MNGI0015 ROS, MNGI0028 NEG, MNGI0009 NEG, MNGI0015 NEG, MNG2829 30, MNGI0033 NEG, MNGI0032 MAR, MNGI0033 MAR, MNGI0001 AZL, MNGI0001 NEG, MNGI0010 CAR, MNG2823 60, MNGI0015 AZL, MNGI0010 AZL, MNG2839 10, MNGI0032 NEG, MNGI0010 NEG, MNGI0001 CAR, MNGI0009 AZL, MNG2838 50, MNGI0027 VER, MNGI0031 AZL
Primary DI / UDI-DI
04895245305142, 04895245305111, 04895245303087, 04895245303421, 04895245304978, 04895245304930, 04895245303414, 04895245304916, 04895245303124, 04895245303131, 04895245303278, 04895245304923, 04895245303018, 04895245303247, 04895245303384, 04895245305098, 04895245305029, 04895245305104, 04895245303230, 04895245303193, 04895245303070, 04895245303360, 04895245303285, 04895245303100, 04895245303407, 04895245305012, 04895245303063, 04895245303209, 04895245303056, 04895245303391, 04895245304909, 04895245305005
Basic UDI-DI
48952453FRMPX6
EMDN Code
Q02100202, Q02100201
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000026315
Authorised representative
MYM SOPORTE TECNICO Y DE CALIDAD, S.L. ES-AR-000017300

Other devices from Everife International Limited

See all devices from Everife International Limited →

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