Simpurity

FDA UDI

Class I (US FDA UDI)

by Safe N Simple Llc

Identity

Trade Name: Simpurity FDA UDI
Generic Name: Woven gauze pad, non-antimicrobial FDA UDI
Device Name: 6 x 6.75 inch Bordered Tefla Pad Gauze Sterile FDA UDI
Model / Reference: SNS52324 FDA UDI
Description: 6 x 6.75 inch Bordered Tefla Pad Gauze Sterile FDA UDI

Identifiers

Catalog Number: SNS52324 FDA UDI
Primary DI / UDI-DI: 00850004779859 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Woven gauze pad, 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 6 Inch FDA UDI
Height — 6.75 Inch FDA UDI

Category: Woven gauze pad, non-antimicrobial

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Safe N Simple Llc

Sources (1)

FDA UDI 8627ba5a-e5c2-4710-9f21-3e2de7af79d3 36 fields · synced Jun 8, 2026