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Certi-Gauze Pads - 4"x 4" - 25/Box

FDA UDI

Class U (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
Certi-Gauze Pads - 4"x 4" - 25/Box FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Certi-Gauze Pads - 4"x 4" - 25/Box FDA UDI
Model / Reference
R231-213 FDA UDI
Description
Certi-Gauze Pads - 4"x 4" - 25/Box FDA UDI

Identifiers

Catalog Number
R231-213 FDA UDI
Primary DI / UDI-DI
00766588312132 FDA UDI
510(k) Number
K945002 FDA UDI
FDA Product Code
EFQ FDA UDI
GMDN Term
Non-woven gauze pad FDA UDI

Classification

Device Class
U 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad

Certi-Gauze Pads - 4"x 4" - 25/Box by Certified Safety Manufacturing, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 052da46f-3a3d-49bc-a5bd-ee605094fa96 36 fields · synced Jun 8, 2026