AincA®

FDA UDI

Class I (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name: AincA® FDA UDI
Generic Name: Low-pressure tubing connector, reusable FDA UDI
Device Name: Tube, Breathing, Semi-Clear Polyester w/Spiral, 9/16" Smooth ID, 36" Long, 22mmF x 22mmF Silicone Ends FDA UDI
Model / Reference: E-215-36 FDA UDI
Description: Tube, Breathing, Semi-Clear Polyester w/Spiral, 9/16" Smooth ID, 36" Long, 22mmF x 22mmF Silicone Ends FDA UDI

Identifiers

Catalog Number: E-215-36 FDA UDI
Primary DI / UDI-DI: B005E215360 FDA UDI
FDA Product Code: BZA FDA UDI
GMDN Term: Low-pressure tubing connector, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5810 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

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Length — 36 Inch FDA UDI

Category: Low-pressure tubing connector, reusable

AincA® by Anesthesia Associates, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Oxygen Tubing Swivel Connectors — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I

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 340f33a5-8d9a-49ec-9808-0ce47a54fa5e 36 fields · synced Jun 8, 2026