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Vyaire

FDA UDI

Class I (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Vyaire FDA UDI
Generic Name
Gas volume reference standard FDA UDI
Device Name
Calibration Syringe 100 ml FDA UDI
Model / Reference
720320 FDA UDI
Description
Calibration Syringe 100 ml FDA UDI

Identifiers

Catalog Number
720320 FDA UDI
Primary DI / UDI-DI
04250892906102 FDA UDI
FDA Product Code
BXW FDA UDI
GMDN Term
Gas volume reference standard FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1870 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Gas volume reference standard

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

Similar devices

Also classified as Gas volume reference standard.

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 c4b90c2c-3532-40fa-8032-462d7c00b6be 35 fields · synced Jun 1, 2026