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Grip-/-L-P-Lf

by Yanga S.r.L EUDAMED

Active European Union

Ref REDIGRIP

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80339542901QZ Basic UDI-DIDate6 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Trade Name
Grip-/-L-P-Lf
Grip-/-C-P-Lf
Grip-/-Kl-P-Lf
Grip-/-K-P-Lf
Grip-/-A-P-Lf
Grip-/-F-P-Lf
Grip-/-G-P-Lf
Grip-/-B-P-Lf
Device Name
Redigrip
Model / Reference
REDIGRIP
Primary DI / UDI-DI
08033954292513, 08033954292421, 08033954292506, 08033954292490, 08033954292407, 08033954292452, 08033954292469, 08033954292414
Basic UDI-DI
80339542901QZ
EMDN Code
M03030201 Tubular mesh
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000053742

Other devices from Yanga S.r.L

See all devices from Yanga S.r.L →

Properties

  • Reprocessed

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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