← Back to catalogue

MicroAire®

FDA UDI

Class II (US FDA UDI)

by MicroAire Surgical Instruments LLC

Identity

Trade Name
MicroAire® FDA UDI
Generic Name
Collection syringe adaptor, single-use FDA UDI
Device Name
SYRINGE ADAPTER, TOOMEY TO LUER FDA UDI
Model / Reference
ASP-ADP-2 FDA UDI
Description
SYRINGE ADAPTER, TOOMEY TO LUER FDA UDI

Identifiers

Primary DI / UDI-DI
00847399006424 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Collection syringe adaptor, single-use 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Collection syringe adaptor, single-use

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

Similar devices

Also classified as Collection syringe adaptor, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 906dad5c-7555-4c51-8d87-3144f72473e9 35 fields · synced Jun 9, 2026