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Aero/Vent Plus

FDA UDI

Class I (US FDA UDI)

by Medi Nuclear Corp., Inc.

Identity

Trade Name
Aero/Vent Plus FDA UDI
Generic Name
Nose clip, single-use FDA UDI
Device Name
Nose Clip, Disposable with Foam Nose Pads FDA UDI
Model / Reference
MN1050 FDA UDI
Description
Nose Clip, Disposable with Foam Nose Pads FDA UDI

Identifiers

Primary DI / UDI-DI
00857863007598 FDA UDI
FDA Product Code
BXJ FDA UDI
GMDN Term
Nose clip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6225 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nose clip, single-use

Aero/Vent Plus by Medi Nuclear Corp., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nose clip, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 934d0a3d-f74e-49b3-8f0a-7a17b01cbead 35 fields · synced May 30, 2026