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Schneider

FDA UDI

Class I (US FDA UDI)

by Avatech Corp.

Identity

Trade Name
Schneider FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Schneider VitaFoam™ Bordered Silicone Foam Adhesive Dressing 3" x 3", 10 Count Per Box FDA UDI
Model / Reference
VF3033RD FDA UDI
Description
Schneider VitaFoam™ Bordered Silicone Foam Adhesive Dressing 3" x 3", 10 Count Per Box FDA UDI

Identifiers

Primary DI / UDI-DI
00198737023505 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 3 Inch FDA UDI
Width — 3 Inch FDA UDI

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

Schneider by Avatech Corp. — Class I — 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
Avatech Corp.

Sources (1)

  • FDA UDI 7f4a31fa-a945-48f0-8c89-0a87ece8290d 36 fields · synced Jun 6, 2026