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Rolled Gauze

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
ROLLED GAUZE FDA UDI
Generic Name
Woven gauze roll/sheet FDA UDI
Device Name
ROLLED GAUZE 1 ea - 4.1 yds x 4.5", six-ply, sterile gauze FDA UDI
Model / Reference
05 FDA UDI
Description
ROLLED GAUZE 1 ea - 4.1 yds x 4.5", six-ply, sterile gauze FDA UDI

Identifiers

Catalog Number
33-300 FDA UDI
Primary DI / UDI-DI
M68933300050 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze roll/sheet 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Woven gauze roll/sheet

Rolled Gauze by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze roll/sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 415a7d5c-938e-4fde-abcb-ea8ef1902a28 35 fields · synced May 30, 2026