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Autoclavable Plastic Ocular Shield, bilateral, large, black 23-206B

by Oculo-Plastik Inc

Ref 23-206

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number697660100US Basic UDI-DI 10697660003105UDI-DIDate7 Feb 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number10697660003105 UDI-DI Date5 Nov 2019ListedStatusListed 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  • Withdrawn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/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Plastic Ocular Shield (large), black EUDAMED
Autoclavable Plastic Ocular Shield, bilateral, large, black GUDID
Generic Name
Radiation/mechanical corneal shield, reusable
Model / Reference
23-206 EUDAMED
23-206B GUDID
Primary DI / UDI-DI
10697660003105
Basic UDI-DI
697660100US
Direct Marketing DI
10697660003105
FDA Product Code
HOY
EMDN Code
T0306 Patient protection devices during clinical procedures
GMDN Term
Radiation/mechanical corneal shield, reusable
Device Class
Class I
Regulation Number
886.4750
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Width — 25.5 Millimeter
Length — 28.5 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
23-206
GUDID
23-206B

Other devices from Oculo-Plastik Inc

See all devices from Oculo-Plastik Inc →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (22)

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