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Vital Signs™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
Vital Signs™ FDA UDI
Generic Name
Electrocardiographic electrode connector FDA UDI
Device Name
Connector for CAM14 Banana V7 Gray AHA FDA UDI
Model / Reference
406554-035 FDA UDI
Description
Connector for CAM14 Banana V7 Gray AHA FDA UDI

Identifiers

Catalog Number
406554-035 FDA UDI
Primary DI / UDI-DI
10190752116931 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic electrode connector

Vital Signs™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 2c47cebc-fdc5-45cc-999e-416e38a3f3f4 36 fields · synced Jun 1, 2026