Merocel™

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name: Merocel™ FDA UDI
Generic Name: Non-woven gauze pad FDA UDI
Device Name: DRESSING 400402 MEROCEL 20PK STD NASAL 8 FDA UDI
Model / Reference: 400402 FDA UDI
Description: DRESSING 400402 MEROCEL 20PK STD NASAL 8 FDA UDI

Identifiers

Primary DI / UDI-DI: 20763000616735 FDA UDI
FDA Product Code: NAB FDA UDI
EFQ 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

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

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 8.0 Centimeter FDA UDI

Category: Non-woven gauze pad

Merocel™ by Medtronic Xomed, 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: Medtronic Xomed, Inc.

Sources (1)

FDA UDI 2c4234c7-1da6-4d8e-be4d-f82f33af4ca5 35 fields · synced May 31, 2026