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Vitale

FDA UDI

Class I (US FDA UDI)

by CellEra, LLC

Identity

Trade Name
Vitale FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Vitale Silicone Composite Dressings, 3.5" x 4", 1/pouch, 30/box, 10 boxes/case FDA UDI
Model / Reference
24204 FDA UDI
Description
Vitale Silicone Composite Dressings, 3.5" x 4", 1/pouch, 30/box, 10 boxes/case FDA UDI

Identifiers

Catalog Number
24204 FDA UDI
Primary DI / UDI-DI
00850005565932 FDA UDI
FDA Product Code
NAD FDA UDI
MGO 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
878.4018 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

No

FDA UDI

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

A wound covering typically in the form of a multi-layered pad having a material or substance on its skin-contact surface, designed to absorb wound blood/exudates while protecting the wound from external contamination and maintaining a moist internal environment.

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
CellEra, LLC

Sources (1)

  • FDA UDI 60b7421d-4eb4-4ad2-8e66-8cfc9270547d 35 fields · synced Jun 19, 2026