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Jmu

FDA UDI

Class I (US FDA UDI)

by Jmu Dental, Inc

Identity

Trade Name
JMU FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
JMU Non-Woven Sponges (4-Ply), 30gsm, 2"X2", 200pcs/bag FDA UDI
Model / Reference
25101001 FDA UDI
Description
JMU Non-Woven Sponges (4-Ply), 30gsm, 2"X2", 200pcs/bag FDA UDI

Identifiers

Primary DI / UDI-DI
00840456214985 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-woven gauze pad

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

Similar devices

Also classified as Non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jmu Dental, Inc

Sources (1)

  • FDA UDI 45be4b30-7234-47e5-871d-cf078f8cbf3e 33 fields · synced Jun 1, 2026