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Xeroform Petrolatum

FDA UDI

by Derma Sciences Canada, Inc

Identity

Trade Name
XEROFORM PETROLATUM FDA UDI
Generic Name
Petrolatum woven gauze pad FDA UDI
Device Name
Petrolatum Dressing. Fine Mesh Gauze Impregnated with 3% Bismuth Tribromophenate in a Petrolatum Blend. FDA UDI
Model / Reference
20068 FDA UDI
Description
Petrolatum Dressing. Fine Mesh Gauze Impregnated with 3% Bismuth Tribromophenate in a Petrolatum Blend. FDA UDI

Identifiers

Catalog Number
DKC20068 FDA UDI
Primary DI / UDI-DI
10381780471318 FDA UDI
FDA Product Code
GER FDA UDI
GMDN Term
Petrolatum woven gauze pad FDA UDI

Classification

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

Dimensions & Sizes

Size
Length — 22.9 Centimeter FDA UDI
Length — 9 Inch FDA UDI
Width — 12.7 Centimeter FDA UDI
Width — 5 Inch FDA UDI

Category: Petrolatum woven gauze pad

Xeroform Petrolatum by Derma Sciences Canada, Inc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Petrolatum woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Derma Sciences Canada, Inc

Sources (1)

  • FDA UDI 65e14138-2a72-4784-86c8-61ac0fb46c9f 37 fields · synced Jun 8, 2026