Jmu

FDA UDI

Class I (US FDA UDI)

by Jmu Dental, Inc

Identity

Trade Name: JMU FDA UDI
Generic Name: General-purpose surgical sponge FDA UDI
Device Name: Sterile Nonwoven Sponge (8-Ply), 2"X2", 1pad/pouch, 100pouches/box FDA UDI
Model / Reference: 25102003 FDA UDI
Description: Sterile Nonwoven Sponge (8-Ply), 2"X2", 1pad/pouch, 100pouches/box FDA UDI

Identifiers

Primary DI / UDI-DI: D930251020030 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: General-purpose surgical sponge 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: General-purpose surgical sponge

Jmu by Jmu Dental, 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: Jmu Dental, Inc

Sources (1)

FDA UDI 80faad94-15fc-40f5-bbe1-0a4583f7699d 33 fields · synced Jun 8, 2026