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MediHoney® 31805

by Acell, Inc.

MediHoney® 31805 is a device classified as Unclassified made by Acell, Inc., listed in FDA GUDID since 14 Sep 2018 (UDI-DI 10381780486978), 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 Number10381780486978 UDI-DI Date14 Sep 2018ListedStatusListed 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  • Withdrawn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
Medical honey liquid barrier dressing
Model / Ref / Catalog
31805
Primary DI / UDI-DI
10381780486978
FDA product code
FRO
GMDN term
Medical honey liquid barrier dressing
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 15 Milliliter
Total Volume — 0.5 Fluid Ounce

Other devices from Acell, Inc.

See all devices from Acell, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)