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Calf Cuff, X-Large

FDA UDI

Class II (US FDA UDI)

by Vasomedical, Inc.

Identity

Trade Name
Calf Cuff, X-Large FDA UDI
Generic Name
External counterpulsation system, stationary FDA UDI
Device Name
Calf Cuff, X-Large FDA UDI
Model / Reference
Model Lumenair FDA UDI
Description
Calf Cuff, X-Large FDA UDI

Identifiers

Catalog Number
V10-0023-5 FDA UDI
Primary DI / UDI-DI
00817980021068 FDA UDI
510(k) Number
K033617 FDA UDI
FDA Product Code
DRN FDA UDI
GMDN Term
External counterpulsation system, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5225 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: External counterpulsation system, stationary

Calf Cuff, X-Large by Vasomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External counterpulsation system, stationary.

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 57b25a6e-d182-4eaf-b574-193472cdf789 36 fields · synced May 30, 2026