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PolyMem

FDA UDI

Class I (US FDA UDI)

by Ferris Mfg. Corp.

Identity

Trade Name
PolyMem FDA UDI
Generic Name
Cavity-wound management dressing, non-antimicrobial FDA UDI
Device Name
1" x 3" WIC Cavity Wound Filler FDA UDI
Model / Reference
WIC FDA UDI
Description
1" x 3" WIC Cavity Wound Filler FDA UDI

Identifiers

Catalog Number
5731 FDA UDI
Primary DI / UDI-DI
10735471057310 FDA UDI
FDA Product Code
KMF FDA UDI
GMDN Term
Cavity-wound management dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cavity-wound management dressing, non-antimicrobial

PolyMem by Ferris Mfg. Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cavity-wound management dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ferris Mfg. Corp.

Sources (1)

  • FDA UDI 02d0e3ad-b270-4dd6-97f7-503b7bd56c83 37 fields · synced Jun 9, 2026