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Stradis Medical, LLC.

FDA UDI

Class II (US FDA UDI)

by Stradis Medical, Llc

Identity

Trade Name
Stradis Medical, LLC. FDA UDI
Generic Name
Wound dressing kit, medicated FDA UDI
Device Name
Dressing Change Kit W/CHG FDA UDI
Model / Reference
HCT8275CP-B FDA UDI
Description
Dressing Change Kit W/CHG FDA UDI

Identifiers

Primary DI / UDI-DI
M752HCT8275CPB0 FDA UDI
FDA Product Code
MCY FDA UDI
GMDN Term
Wound dressing kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound dressing kit, medicated

Stradis Medical, LLC. by Stradis Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound dressing kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 666e4250-7ae1-43e7-b858-f1ace43de519 34 fields · synced May 30, 2026