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Boston Scientific

FDA UDI

Class II (US FDA UDI)

by Nissha Medical Technologies Sas

Identity

Trade Name
Boston Scientific FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Trunk Cable ECG CLEARSIGN AAMI 6m FDA UDI
Model / Reference
BS-71041-US-60 FDA UDI
Description
Trunk Cable ECG CLEARSIGN AAMI 6m FDA UDI

Identifiers

Catalog Number
M004BS71041US60 FDA UDI
Primary DI / UDI-DI
03700506320363 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic lead set, reusable 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

Category: Electrocardiographic lead set, reusable

Boston Scientific by Nissha Medical Technologies Sas — 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 9171c4fa-ce8e-47fb-bbe5-2bc80c027d0f 35 fields · synced Jun 1, 2026