MicroAire®

FDA UDI

Class II (US FDA UDI)

by MicroAire Surgical Instruments LLC

Identity

Trade Name: MicroAire® FDA UDI
Generic Name: Methoxyflurane anaesthesia vaporizer FDA UDI
Device Name: VACUUM TUBING, 4PK, 5/8"OD x 3/8"ID x 3FT FDA UDI
Model / Reference: ASP-TUBING FDA UDI
Description: VACUUM TUBING, 4PK, 5/8"OD x 3/8"ID x 3FT FDA UDI

Identifiers

Primary DI / UDI-DI: 00847399018960 FDA UDI
510(k) Number: K242804 FDA UDI
FDA Product Code: QPB FDA UDI
GMDN Term: Methoxyflurane anaesthesia vaporizer FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.5040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 0.625 Inch FDA UDI
Lumen/Inner Diameter — 0.375 Inch FDA UDI
Length — 3 Feet FDA UDI

Category: Methoxyflurane anaesthesia vaporizer

MicroAire® by MicroAire Surgical Instruments LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K242804 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: MicroAire Surgical Instruments LLC

Sources (1)

FDA UDI a77ae725-385c-4159-bd9c-90d541a6376b 36 fields · synced Jun 9, 2026