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Xeroform

FDA UDI

Class U (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Xeroform FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Non-occlusive Roll,3% Bismuth Tribromophenate in Oil Emulsion FDA UDI
Model / Reference
8884437305 FDA UDI
Description
Non-occlusive Roll,3% Bismuth Tribromophenate in Oil Emulsion FDA UDI

Identifiers

Catalog Number
8884437305 FDA UDI
Primary DI / UDI-DI
10884527014996 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-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

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 — 9 Feet FDA UDI
Width — 4 Inch FDA UDI

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

Xeroform by Cardinalhealth — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 7224c25d-86e9-4a56-9ecb-5a2fa0dc8783 37 fields · synced May 31, 2026