MicroAire®

FDA UDI

Class II (US FDA UDI)

by MicroAire Surgical Instruments LLC

Identity

Trade Name: MicroAire® FDA UDI
Generic Name: Surgical instrument protective cap FDA UDI
Device Name: WASHER DISINFECTOR CAP, MICROAIRE STYLE CONNECTOR FDA UDI
Model / Reference: CAP-100 FDA UDI
Description: WASHER DISINFECTOR CAP, MICROAIRE STYLE CONNECTOR FDA UDI

Identifiers

Primary DI / UDI-DI: 00847399006622 FDA UDI
FDA Product Code: KCT FDA UDI
GMDN Term: Surgical instrument protective cap FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6850 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument protective cap

MicroAire® by MicroAire Surgical Instruments LLC — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: MicroAire Surgical Instruments LLC

Sources (1)

FDA UDI e1c00265-c423-45e9-9fbd-8ae3b53ee83d 34 fields · synced Jun 9, 2026