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OmniTrustTM

FDA UDI

Class I (US FDA UDI)

by Omni International Corp.

Identity

Trade Name
OmniTrustTM FDA UDI
Generic Name
Wound compression dressing FDA UDI
Device Name
ABD Combine Dressing, Sterile, 8x7.5 FDA UDI
Model / Reference
9071-87 FDA UDI
Description
ABD Combine Dressing, Sterile, 8x7.5 FDA UDI

Identifiers

Catalog Number
9071-87 FDA UDI
Primary DI / UDI-DI
00810572006351 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Wound compression dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI
Width — 7.5 Inch FDA UDI

Category: Wound compression dressing

OmniTrustTM by Omni International Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound compression dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85c5d784-850b-458f-99cf-acf513d9f4b5 36 fields · synced May 30, 2026