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Petroleum Gauze Dressing, Non-Woven

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Petroleum Gauze Dressing, Non-Woven FDA UDI
Generic Name
Petrolatum non-woven gauze pad FDA UDI
Device Name
Med-High Absorbency For wound stages 2, 3, 4 Sterile FDA UDI
Model / Reference
3041 FDA UDI
Description
Med-High Absorbency For wound stages 2, 3, 4 Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00840117324213 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Petrolatum non-woven gauze pad 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Petrolatum non-woven gauze pad

Petroleum Gauze Dressing, Non-Woven by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Petrolatum non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 01e78868-2d8b-466b-9f1f-1b081a35cbb2 33 fields · synced May 31, 2026