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Jaeger

FDA UDI

Class II (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Jaeger FDA UDI
Generic Name
Pulmonary function analysis system, adult FDA UDI
Device Name
Double tube adapter with In/Ex-valve FDA UDI
Model / Reference
706134 FDA UDI
Description
Double tube adapter with In/Ex-valve FDA UDI

Identifiers

Catalog Number
706134 FDA UDI
Primary DI / UDI-DI
14250892902156 FDA UDI
510(k) Number
K122699 FDA UDI
FDA Product Code
BZC FDA UDI
GMDN Term
Pulmonary function analysis system, adult FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1880 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Cleared under the same submission

K122699 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 7f2bd8d5-77ec-401c-8ce6-c9d1818527d7 38 fields · synced Jun 8, 2026