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MediHoney®

FDA UDI

Class U (US FDA UDI)

by Acell, Inc.

Identity

Trade Name
MediHoney® FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, antimicrobial FDA UDI
Device Name
MEDIHONEY® (ADHESIVE) HYDROGEL COLLOIDAL SHEET with LEPTOSPERMUM HONEY WOUND & BURN DRESSING FDA UDI
Model / Reference
31738 FDA UDI
Description
MEDIHONEY® (ADHESIVE) HYDROGEL COLLOIDAL SHEET with LEPTOSPERMUM HONEY WOUND & BURN DRESSING FDA UDI

Identifiers

Catalog Number
31738 FDA UDI
Primary DI / UDI-DI
10381780486961 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, antimicrobial FDA UDI

Classification

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

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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: Wound-nonadherent dressing, permeable, antimicrobial

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

Similar devices

Also classified as Wound-nonadherent dressing, permeable, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acell, Inc.

Sources (1)

  • FDA UDI 6c971a31-46b7-4d61-b408-4b0fe38ee703 37 fields · synced Jun 6, 2026