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USB SD Card Reader

FDA UDI

Class II (US FDA UDI)

by Vasomedical, Inc.

Identity

Trade Name
USB SD Card Reader FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
USB SD Card Reader FDA UDI
Model / Reference
Model 1303 FDA UDI
Description
USB SD Card Reader FDA UDI

Identifiers

Catalog Number
A10-0015 FDA UDI
Primary DI / UDI-DI
00817980020597 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

USB SD Card Reader 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 0bda696a-720a-4d31-860d-0eeefd8c0eb6 36 fields · synced Jun 8, 2026