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Portable case with Belt for 2301/2302 Recorders

FDA UDI

Class II (US FDA UDI)

by Vasomedical, Inc.

Identity

Trade Name
Portable case with Belt for 2301/2302 Recorders FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
Portable case with Belt for 2301/2302 Recorders FDA UDI
Model / Reference
Model 2301 FDA UDI
Description
Portable case with Belt for 2301/2302 Recorders FDA UDI

Identifiers

Catalog Number
A10-0043 FDA UDI
Primary DI / UDI-DI
00817980020641 FDA UDI
510(k) Number
K111180 FDA UDI
FDA Product Code
DSH FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2800 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic lead set, reusable

Portable case with Belt for 2301/2302 Recorders by Vasomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vasomedical, Inc.

Sources (1)

  • FDA UDI 82200a75-a1fc-49e0-9bfd-cdc5973ffcfe 36 fields · synced May 30, 2026