← Back to catalogue

AincA®

FDA UDI

Class I (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Breathing circuit tube holder FDA UDI
Device Name
Protector, Arm (BP, IV, Press. Lines), Wells Type Curved, Under Table Pad, Aluminum FDA UDI
Model / Reference
00-417 FDA UDI
Description
Protector, Arm (BP, IV, Press. Lines), Wells Type Curved, Under Table Pad, Aluminum FDA UDI

Identifiers

Catalog Number
00-417 FDA UDI
Primary DI / UDI-DI
B005004170 FDA UDI
FDA Product Code
JAY FDA UDI
GMDN Term
Breathing circuit tube holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5280 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breathing circuit tube holder

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

Similar devices

Also classified as Breathing circuit tube holder.

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 3dab71c6-77a0-416b-8ff7-7f06e31cf131 35 fields · synced May 30, 2026