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Rylon 5x5

FDA UDI

Class I (US FDA UDI)

by Bio Med Sciences, Inc.

Identity

Trade Name
Rylon 5x5 FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
Device Name
Single-Sided Non-Adherent Wound Dressing FDA UDI
Model / Reference
2325.1 FDA UDI
Description
Single-Sided Non-Adherent Wound Dressing FDA UDI

Identifiers

Catalog Number
2325.1 FDA UDI
Primary DI / UDI-DI
00810050460071 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Dimensions & Sizes

Size
Width — 5 Inch FDA UDI
Length — 5 Inch FDA UDI
Width — 13 Centimeter FDA UDI
Length — 13 Centimeter FDA UDI

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

Rylon 5x5 by Bio Med Sciences, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, permeable, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio Med Sciences, Inc.

Sources (1)

  • FDA UDI 994fd580-906b-4be1-a4e7-9738f79bc3c3 36 fields · synced Jun 8, 2026