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PolyMem

FDA UDI

Class I (US FDA UDI)

by Ferris Mfg. Corp.

Identity

Trade Name
PolyMem FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
#8 Oval PolyMem Silicone Border Dressing FDA UDI
Model / Reference
Silicone Border FDA UDI
Description
#8 Oval PolyMem Silicone Border Dressing FDA UDI

Identifiers

Catalog Number
2468 FDA UDI
Primary DI / UDI-DI
10735471024688 FDA UDI
FDA Product Code
KMF FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, 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

Yes

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: Wound-nonadherent dressing, absorbent, non-antimicrobial

PolyMem by Ferris Mfg. 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
Ferris Mfg. Corp.

Sources (1)

  • FDA UDI bcd8e9b5-cc02-403e-9021-3b59bf7327f4 37 fields · synced Jun 9, 2026