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Mask Adapter

FDA UDI

Class II (US FDA UDI)

by Omron Healthcare, Inc.

Identity

Trade Name
Mask Adapter FDA UDI
Generic Name
Nebulizing system delivery set, reusable FDA UDI
Device Name
Mask Adapter for NE-U100 (MicroAir Vibrating Mesh Nebulizer) FDA UDI
Model / Reference
U100-2 FDA UDI
Description
Mask Adapter for NE-U100 (MicroAir Vibrating Mesh Nebulizer) FDA UDI

Identifiers

Catalog Number
U100-2 FDA UDI
Primary DI / UDI-DI
00073796011024 FDA UDI
510(k) Number
K062263 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Nebulizing system delivery set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nebulizing system delivery set, reusable

Mask Adapter by Omron Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 383d461b-a75a-4bee-b1c0-d8e906cc36e2 36 fields · synced Jun 8, 2026