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LMP Manuka Foam Air

FDA UDI

Class U (US FDA UDI)

by Links Medical Products, Inc.

Identity

Trade Name
LMP Manuka Foam Air FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Honey-impregnated foam wound dressing FDA UDI
Model / Reference
WC70 FDA UDI
Description
Honey-impregnated foam wound dressing FDA UDI

Identifiers

Catalog Number
WC70 FDA UDI
Primary DI / UDI-DI
00851028001407 FDA UDI
510(k) Number
K133934 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-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

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

Dimensions & Sizes

Size
Height — 4 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

LMP Manuka Foam Air by Links Medical Products, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f73d40fb-e9d3-4c61-9379-e23e73923d82 38 fields · synced Sep 18, 2026