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Finger Plethysmograph - MC2

FDA UDI

Class II (US FDA UDI)

by Vasomedical, Inc.

Identity

Trade Name
Finger Plethysmograph (Model MC2, AngioNew® V& VI) FDA UDI
Generic Name
Plethysmography phototransducer FDA UDI
Device Name
Finger Plethysmograph (Model MC2, AngioNew® V& VI) FDA UDI
Model / Reference
Model AngioNew VI FDA UDI
Description
Finger Plethysmograph (Model MC2, AngioNew® V& VI) FDA UDI

Identifiers

Catalog Number
V23-0007 FDA UDI
Primary DI / UDI-DI
00817980021204 FDA UDI
510(k) Number
K033617 FDA UDI
FDA Product Code
DRN FDA UDI
GMDN Term
Plethysmography phototransducer FDA UDI
Models / Variants
MC2 FDA UDI
AngioNew® V FDA UDI
VI) 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: Plethysmography phototransducer

Finger Plethysmograph - MC2 by Vasomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 3 models — regulatory data on deviCERTS

Similar devices

Also classified as Plethysmography phototransducer.

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 4c196a74-4c6c-4876-9e5a-769fd8fbbd2e 36 fields · synced May 30, 2026