AincA®

FDA UDI

Class I (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name: AincA® FDA UDI
Generic Name: Oropharyngeal airway, single-use FDA UDI
Device Name: Airway, Intubator, Williams Type-10cm, (Max ETT: 8.5mmID), Pink (10/Pkg), Disposable Plastic FDA UDI
Model / Reference: 00-486 FDA UDI
Description: Airway, Intubator, Williams Type-10cm, (Max ETT: 8.5mmID), Pink (10/Pkg), Disposable Plastic FDA UDI

Identifiers

Catalog Number: 00-486 FDA UDI
Primary DI / UDI-DI: B005004863 FDA UDI
FDA Product Code: CAE FDA UDI
GMDN Term: Oropharyngeal airway, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5110 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

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Length — 10 Centimeter FDA UDI

Category: Oropharyngeal airway, single-use

AincA® by Anesthesia Associates, 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: Anesthesia Associates, Inc.

Sources (1)

FDA UDI 193abcc0-4bca-46ac-a17c-c9373304b23a 36 fields · synced May 31, 2026