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AincA®

FDA UDI

Class I (US FDA UDI)

by Anesthesia Associates, Inc.

Identity

Trade Name
AincA® FDA UDI
Generic Name
Mechanical external stethoscope FDA UDI
Device Name
Chest Piece, MRI, Child, Lightweight (1.12"OD, 0.3"H), LuerM, Delrin/Nylon FDA UDI
Model / Reference
00-542 FDA UDI
Description
Chest Piece, MRI, Child, Lightweight (1.12"OD, 0.3"H), LuerM, Delrin/Nylon FDA UDI

Identifiers

Catalog Number
00-542 FDA UDI
Primary DI / UDI-DI
B005005420 FDA UDI
FDA Product Code
BZS FDA UDI
GMDN Term
Mechanical external stethoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1930 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
MRI Safety
MR Safe FDA UDI

Category: Mechanical external stethoscope

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

Similar devices

Also classified as Mechanical external stethoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anesthesia Associates, Inc.

Sources (1)

  • FDA UDI fa87c205-b817-4479-b29a-d9de6560c728 36 fields · synced May 31, 2026