Vyntus

DVT Adapter w. salvia trap

Registry build 21.09.26
1manufacturer
14catalogue numbers in this listing
1recall

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code BZC
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77

Record

Regulatory record for Vyntus
Listed by Jaeger Medical GmbH, Germany
FDA product code BZC
Device type Calculator, Pulmonary Function Data
Device class Class 2
Regulation 21 CFR 868.1880
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K150810
Record published 2018-07-31
Record revised 2025-05-28 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, manufacturing date, serial number
Storage Storage environment humidity 15 to 95 % RH; Storage environment temperature -20 to 50 °C
Distribution end date 2020-07-29

Catalogue Numbers

Catalogue numbers for Vyntus
Catalogue number Size Status
V-178699 In distribution
V-859215 Withdrawn
V-178600-13 Withdrawn
V-707329 Withdrawn
V-707708 Withdrawn
852828 Withdrawn
V-707326 Withdrawn
V-178602 Withdrawn
V-178601 Withdrawn
V-178603 Withdrawn
V-821555 Withdrawn
V-707327 Withdrawn
V-859210 Withdrawn
V-835490 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Jaeger Jaeger Medical GmbH 227
Vyaire Jaeger Medical GmbH 120
Innocor Innovision Medical Technologies, LLC 6
Vyntus Vyaire Medical, Inc. 3
Cosmed C O S M E D SRL 3
APS-Pro SA Jaeger Medical GmbH 3
MGC Diagnostics Medical Graphics Corp. 2
TransAir3 Medi Soft SA 1
MasterScreen PFT Jaeger Medical GmbH 1
Respiratory Mechanics Sensor → Neonatal Draeger Medical Systems, Inc. 1
SentrySuite Software Jaeger Medical GmbH 1
TrueOne 2400 Parvomedics, Incorporated 1

Showing 12 of 19. All products under Calculator, Pulmonary Function Data

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Vyntus
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Jaeger Medical GmbH 510(k) number 2024-04-08 Class I Process control Potential of the nozzle separating during patient use. 649 devices

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer