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Medihoney®

FDA UDI

Class U (US FDA UDI)

by Acell, Inc.

Identity

Trade Name
MEDIHONEY® FDA UDI
Generic Name
Medical honey liquid barrier dressing FDA UDI
Device Name
MEDIHONEY® Gel Dressing with Active Leptospermum Honey FDA UDI
Model / Reference
31840 FDA UDI
Description
MEDIHONEY® Gel Dressing with Active Leptospermum Honey FDA UDI

Identifiers

Catalog Number
31840 FDA UDI
Primary DI / UDI-DI
10381780486893 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Medical honey liquid barrier dressing FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical honey liquid barrier dressing

Medihoney® by Acell, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical honey liquid barrier dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acell, Inc.

Sources (1)

  • FDA UDI 8aab7a5c-4207-46e7-a1a6-9eee315ec5c5 37 fields · synced May 31, 2026