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Conformant 2 Wnd Vl12x12 Cs48

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
CONFORMANT 2 WND VL12X12 CS48 FDA UDI
Generic Name
Synthetic polymer fluid-permeable film dressing FDA UDI
Device Name
Polyethylene wound contact layer FDA UDI
Model / Reference
59551212 FDA UDI
Description
Polyethylene wound contact layer FDA UDI

Identifiers

Catalog Number
59551212 FDA UDI
Primary DI / UDI-DI
00040565119328 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Synthetic polymer fluid-permeable film dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

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

No

FDA UDI

Category: Synthetic polymer fluid-permeable film dressing

Conformant 2 Wnd Vl12x12 Cs48 by Smith & Nephew Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic polymer fluid-permeable film dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew Medical, Ltd.

Sources (1)

  • FDA UDI 0385d30f-e672-487e-9276-5d0ec56a3773 34 fields · synced Jun 1, 2026