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Dermapure

FDA UDI

Class U (US FDA UDI)

by Safe N Simple Llc

Identity

Trade Name
Dermapure FDA UDI
Generic Name
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI
Device Name
Dermapure Wound Cleanser 8 ounce Bottle FDA UDI
Model / Reference
SNS51118 FDA UDI
Description
Dermapure Wound Cleanser 8 ounce Bottle FDA UDI

Identifiers

Catalog Number
SNS51118 FDA UDI
Primary DI / UDI-DI
00850004779484 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 8 Fluid Ounce FDA UDI

Category: Non-antimicrobial wound irrigation solution, multiple solute

Dermapure by Safe N Simple Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-antimicrobial wound irrigation solution, multiple solute.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Safe N Simple Llc

Sources (1)

  • FDA UDI 95175854-4784-4c6e-a245-54a58e87da7f 36 fields · synced May 30, 2026