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Patterson

FDA UDI

Class I (US FDA UDI)

by Patterson Dental Supply, Inc.

Identity

Trade Name
Patterson FDA UDI
Generic Name
Non-woven gauze pad, non-sterile FDA UDI
Device Name
Patterson® Nonwoven Gauze Sponges – Nonsterile, 4 ply 2 x 2 5000/Case FDA UDI
Model / Reference
070896167 FDA UDI
Description
Patterson® Nonwoven Gauze Sponges – Nonsterile, 4 ply 2 x 2 5000/Case FDA UDI

Identifiers

Primary DI / UDI-DI
D6620708961674 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Non-woven gauze pad, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad, non-sterile

Patterson by Patterson Dental Supply, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f2c77e63-11bf-4d56-a25c-5842c3301ff0 33 fields · synced May 30, 2026