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Excilon

FDA UDI

Class U (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Excilon FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Excilon AMD Antimicrobial Drain Sponges 6 Ply • 0.2 percent Polyhexamethylene Biguanide HCl (PHMB) Kills bacteria like Staph & MRSA 4 x 4 in. (10.2 x 10.2 cm) FDA UDI
Model / Reference
7088 FDA UDI
Description
Excilon AMD Antimicrobial Drain Sponges 6 Ply • 0.2 percent Polyhexamethylene Biguanide HCl (PHMB) Kills bacteria like Staph & MRSA 4 x 4 in. (10.2 x 10.2 cm) FDA UDI

Identifiers

Catalog Number
7088 FDA UDI
Primary DI / UDI-DI
20192253047209 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-woven gauze pad 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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 — 4 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Non-woven gauze pad

Excilon by Cardinal Health 200, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3128259-25d5-4558-9a29-e80eeb2919a1 35 fields · synced Jun 8, 2026