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Snap Electrodes, 90"

FDA UDI

Class II (US FDA UDI)

by Braebon Medical Corp.

Identity

Trade Name
Snap Electrodes, 90" FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Leadwires for snap electrodes. FDA UDI
Model / Reference
8621-90 FDA UDI
Description
Leadwires for snap electrodes. FDA UDI

Identifiers

Catalog Number
8621-90 FDA UDI
Primary DI / UDI-DI
B1408621901 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 90 Inch FDA UDI

Category: Electrocardiographic lead set, reusable

Snap Electrodes, 90" by Braebon Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 42e751c7-23e9-46d3-9048-e214d7c4b394 36 fields · synced May 30, 2026