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Visitec 0008601

by Beaver-Visitec International Inc

Visitec 0008601 is a Class I device made by Beaver-Visitec International Inc, listed in FDA GUDID since 6 Jun 2024 (UDI-DI 30886158010358), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30886158010358 UDI-DI Date6 Jun 2024ListedStatusListed 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  • Withdrawn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
Visitec
Generic name
Eye patch, single-use
Model / Ref / Catalog
0008601
Primary DI / UDI-DI
30886158010358
FDA product code
HOY
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye patch

Similar devices in this category

Other devices filed under Eye patch.

Other devices from Beaver-Visitec International Inc

See all devices from Beaver-Visitec International Inc →

Properties

  • Premarket exempt
Other properties (14, all answered No)