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Aero/Vent Plus

FDA UDI

Class II (US FDA UDI)

by Medi Nuclear Corp., Inc.

Identity

Trade Name
Aero/Vent Plus FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
Lead Adapter Replacement, Powder coated lead adapter with 7 ft. oxygen tube with secure fit connector FDA UDI
Model / Reference
AV-1010 FDA UDI
Description
Lead Adapter Replacement, Powder coated lead adapter with 7 ft. oxygen tube with secure fit connector FDA UDI

Identifiers

Primary DI / UDI-DI
00857863007918 FDA UDI
510(k) Number
K865107 FDA UDI
FDA Product Code
IYT FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1390 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oxygen administration tubing

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

Similar devices

Also classified as Oxygen administration tubing.

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 fc627721-25ce-4265-a36e-1780ffdc5e8f 36 fields · synced May 30, 2026