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MediHoney® 31738

by Acell, Inc.

MediHoney® 31738 is a device classified as Unclassified made by Acell, Inc., listed in FDA GUDID since 7 Mar 2019 (UDI-DI 10381780486961), 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 Number10381780486961 UDI-DI Date7 Mar 2019ListedStatusListed 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  • Withdrawn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
MediHoney®
Generic name
Wound-nonadherent dressing, permeable, antimicrobial
Model / Ref / Catalog
31738
Primary DI / UDI-DI
10381780486961
FDA product code
FRO
GMDN term
Wound-nonadherent dressing, permeable, antimicrobial
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wound-nonadherent dressing, permeable, antimicrobial

Similar devices

Other devices filed under FDA product code FRO (Dressing, wound, drug).

Other devices from Acell, Inc.

See all devices from Acell, Inc. →

Properties

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