← Back to catalogue

Simpurity

FDA UDI

Class I (US FDA UDI)

by Safe N Simple Llc

Identity

Trade Name
Simpurity FDA UDI
Generic Name
Wound hydrogel dressing, non-antimicrobial FDA UDI
Device Name
Hydrogel Dressing 2 x 2 inch FDA UDI
Model / Reference
SNS58302 FDA UDI
Description
Hydrogel Dressing 2 x 2 inch FDA UDI

Identifiers

Catalog Number
SNS58302 FDA UDI
Primary DI / UDI-DI
00856253007675 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 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

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Height — 2 Inch FDA UDI
Length — 2 Inch FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

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

Similar devices

Also classified as Wound hydrogel dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Safe N Simple Llc

Sources (1)

  • FDA UDI e4966827-4dae-4775-82df-2cf229cada7b 36 fields · synced May 30, 2026