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Grafco 1273

by GF Health Products, Inc.

Grafco 1273 is a Class I device made by GF Health Products, Inc., listed in FDA GUDID since 1 Oct 2020 (UDI-DI M36812731), 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 NumberM36812731 UDI-DI Date1 Oct 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Grafco
Generic name
Eye patch, single-use
Model / Ref / Catalog
1273
Primary DI / UDI-DI
M36812731
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 GF Health Products, Inc.

See all devices from GF Health Products, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)