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Pro-ophta@ Ocular Sticks

by Lohmann & Rauscher International GmbH & Co KG

Pro-ophta@ Ocular Sticks (16515) is a Class II device made by Lohmann & Rauscher International GmbH & Co KG, listed in FDA GUDID since 17 Oct 2016 (UDI-DI 04021447165158), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04021447165158 UDI-DI Date17 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pro-ophta@
Generic name
Ophthalmic sponge
Model / Ref / Catalog
Ocular Sticks, 16515
Primary DI / UDI-DI
04021447165158
FDA product code
HOZ
GMDN term
Ophthalmic sponge
Device class
Class II
Regulation number
886.4790
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Ophthalmic sponge.

Other devices from Lohmann & Rauscher International GmbH & Co KG

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)