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DuCare®

FDA UDI

Class I (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
DuCare® FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
4 in X 4 in 12 ply, 20 X 10 mesh gauze sponge. Sterile FDA UDI
Model / Reference
82410 FDA UDI
Description
4 in X 4 in 12 ply, 20 X 10 mesh gauze sponge. Sterile FDA UDI

Identifiers

Catalog Number
DUP82410 FDA UDI
Primary DI / UDI-DI
00809958084113 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

DuCare® by Derma Sciences Canada, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

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 23d3094a-360d-4079-a94e-74a9ccb4f47b 36 fields · synced May 30, 2026