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Medline MDG44220368

by Medline Industries, Inc.

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

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

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10080196284283 UDI-DI Date27 Jan 2022ListedStatusListed 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  • Withdrawn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
Medline
Generic Name
Hand-held surgical retractor, reusable
Model / Ref / Catalog
MDG44220368
Primary DI / UDI-DI
10080196284283
FDA Product Code
GEI
GMDN Term
Hand-held surgical retractor, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hand-held surgical retractor, reusable

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

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