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: Aerosol face mask, rebreathing, single-use FDA UDI
Device Name: Face Mask, Air-Cushioned, Adult Size 5, 22mm ID FDA UDI
Model / Reference: MN5045 FDA UDI
Description: Face Mask, Air-Cushioned, Adult Size 5, 22mm ID FDA UDI

Identifiers

Primary DI / UDI-DI: 00857863007468 FDA UDI
FDA Product Code: BSJ FDA UDI
GMDN Term: Aerosol face mask, rebreathing, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5550 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Category: Aerosol face mask, rebreathing, single-use

Aero/Vent Plus by Medi Nuclear Corp., 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: Medi Nuclear Corp., Inc.

Sources (1)

FDA UDI f9642eb7-c265-4e2b-9eca-99af81e15752 35 fields · synced May 30, 2026