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Stradis Medical, LLC.

FDA UDI

by Stradis Medical, Llc

Identity

Trade Name
Stradis Medical, LLC. FDA UDI
Generic Name
Wound dressing kit, non-medicated FDA UDI
Device Name
DRESSING CHANGE KIT (3mL) W/RED BAG FDA UDI
Model / Reference
BRF-060MSP201DC FDA UDI
Description
DRESSING CHANGE KIT (3mL) W/RED BAG FDA UDI

Identifiers

Primary DI / UDI-DI
M752BRF060MSP201DC0 FDA UDI
GMDN Term
Wound dressing kit, non-medicated FDA UDI

Classification

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, non-medicated

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

Similar devices

Also classified as Wound dressing kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 14308010-4749-4c70-b851-4f9e0b789e06 34 fields · synced May 30, 2026