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ALGICELL® Ag

FDA UDI

Class U (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
ALGICELL® Ag FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, antimicrobial FDA UDI
Device Name
ALGICELL AG CALCIUM ALGINATE SILVER 2"X 2" FDA UDI
Model / Reference
88522 FDA UDI
Description
ALGICELL AG CALCIUM ALGINATE SILVER 2"X 2" FDA UDI

Identifiers

Catalog Number
DUP88522 FDA UDI
Primary DI / UDI-DI
00809958187951 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Exudate-absorbent dressing, hydrophilic-gel, antimicrobial

ALGICELL® Ag by Derma Sciences Canada, Inc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, 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 9d4ae65d-cd9a-403a-b0ab-2d1bbed9650c 34 fields · synced May 30, 2026