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Jaeger

FDA UDI

Class II (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Jaeger FDA UDI
Generic Name
Cardiopulmonary stress exercise monitoring system FDA UDI
Device Name
Triple-V complete FDA UDI
Model / Reference
707230 FDA UDI
Description
Triple-V complete FDA UDI

Identifiers

Catalog Number
707230 FDA UDI
Primary DI / UDI-DI
14250892907458 FDA UDI
510(k) Number
K072323 FDA UDI
FDA Product Code
BZC FDA UDI
GMDN Term
Cardiopulmonary stress exercise monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1880 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiopulmonary stress exercise monitoring system

Jaeger by Jaeger Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary stress exercise monitoring system.

Cleared under the same submission

K072323 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jaeger Medical GmbH

Sources (1)

  • FDA UDI 09d68088-0c65-4df2-8254-10a08b7d9d73 37 fields · synced Jun 6, 2026