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Crawford 28-0184

by JEDMED Instrument Company

Crawford 28-0184 is a device classified as Unclassified made by JEDMED Instrument Company, listed in FDA GUDID since 14 Dec 2016 (UDI-DI M6332801840), 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 NumberM6332801840 UDI-DI Date14 Dec 2016ListedStatusListed 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  • Withdrawn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
Crawford
Generic name
Lacrimal intubation set
Model / Ref / Catalog
28-0184
Primary DI / UDI-DI
M6332801840
FDA product code
OKS
GMDN term
Lacrimal intubation set
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Lacrimal intubation set

Other devices from JEDMED Instrument Company

See all devices from JEDMED Instrument Company →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)