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Laminar OPOHF21L

by Johnson & Johnson Surgical Vision, Inc.

Ref OPOHF21L

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

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
European UnionCE/MDD EUDAMED NumberB-USMF00003896800210565 Basic UDI-DI D-USMF00003896800210565UDI-DIDate30 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-USMF00003896800210565 UDI-DI Date2 Sep 2016ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Laminar
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Model / Ref / Catalog
OPOHF21L
Primary DI / UDI-DI
D-USMF00003896800210565 EUDAMED
05050474573376 GUDID
Basic UDI-DI
B-USMF00003896800210565
FDA Product Code
HQC
EMDN Code
Q020699 Phacoemulsification devices - other
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
886.4670
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D-USMF00003896800210565
GUDID
05050474573376
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Other devices from Johnson & Johnson Surgical Vision, Inc.

See all devices from Johnson & Johnson Surgical Vision, Inc. →

Properties

  • Sterile
  • Reusable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Single Use: No
  • Implantable: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No