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Artificial Iris with Fiber Select Dark Green

by HumanOptics Holding AG Germany EUDAMEDGUDID

Ref 00095181 Product code QBTEMDN P0399

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number04049154169474 UDI-DIDate1 Jul 2026ListedStatusIn distribution
European UnionCE/MDR EUDAMED Number44911221836 Date10 Jun 2026IssuedStatusActive expires 12 Jun 2030

Coverage

2 jurisdictions

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 44911221836 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0044
    Issued
    10 Jun 2026
    Expires
    12 Jun 2030
    Reason
    Other
  • 44912221836 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 0044
    Issued
    10 Jun 2026
    Expires
    12 Jun 2030
    Reason
    Other

Specification

EUDAMED · GUDID · synced 23 Oct 2026

Generic Name
Implantable iris prosthesis
Model / Ref / Catalog
00095181, 95181
Primary DI / UDI-DI
04049154169474
Basic UDI-DI
04049154_AI_M1_H1_O1_X7
PMA Number
FDA Product Code
QBT
EMDN Code
P0399 Ocular prostheses - other
GMDN Term
Implantable iris prosthesis
Device Class
Class IIb EUDAMED
Class III GUDID
Market of Registration
Germany
Commercial Distribution
In Commercial Distribution
MRI Safety
MR Unsafe
Size
Outer Diameter — 12.8 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
00095181
GUDID
95181
Device ClassEUDAMED
Class IIb
GUDID
Class III

Manufacturer details

EUDAMED SRN
DE-MF-000017892

Other devices from HumanOptics Holding AG

See all devices from HumanOptics Holding AG →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date
Other properties (19)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No

Sources (2)

  • EUDAMED cd665461-a01a-434b-b016-e3de5f816bd5 61 fields · synced 22 Oct 2026
  • FDA UDI a361e4c4-e3c6-42df-be08-a8a0013a316e 37 fields · synced 23 Oct 2026