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MedVance

FDA UDI

Class I (US FDA UDI)

by Med Way Inc.

Identity

Trade Name
MedVance FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI
Device Name
Bordered Hydrocolloid dressing 3.5x5 inches FDA UDI
Model / Reference
V2213505 FDA UDI
Description
Bordered Hydrocolloid dressing 3.5x5 inches FDA UDI

Identifiers

Primary DI / UDI-DI
00857544007640 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, 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

No

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
Sterilization Method
Radiation Sterilization FDA UDI

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

MedVance by Med Way Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Way Inc.

Sources (1)

  • FDA UDI 091c16d9-077b-4a27-8a7f-74921474fbf5 33 fields · synced May 30, 2026