Sterilux Gz Sponge St 4x4 12ply 1200/Cs

FDA UDI

Class I (US FDA UDI)

by Hartmann Usa Inc.

Identity

Trade Name: STERILUX GZ SPONGE ST 4X4 12PLY 1200/CS FDA UDI
Generic Name: Woven gauze pad, non-antimicrobial FDA UDI
Device Name: STERILUX GZ SPONGE ST 4X4 12PLY 1200/CS FDA UDI
Model / Reference: 56910000 FDA UDI
Description: STERILUX GZ SPONGE ST 4X4 12PLY 1200/CS FDA UDI

Identifiers

Primary DI / UDI-DI: 10612553015430 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

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

Category: Woven gauze pad, non-antimicrobial

Sterilux Gz Sponge St 4x4 12ply 1200/Cs by Hartmann Usa Inc. — 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: Hartmann Usa Inc.

Sources (1)

FDA UDI a4d8b7f2-056f-4e25-b7aa-0f171c06e77a 33 fields · synced May 30, 2026