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Vamos 2

FDA UDI

Class II (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
Vamos 2 FDA UDI
Generic Name
Anaesthetic agent gas monitor, multiple FDA UDI
Model / Reference
6871990 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675227489 FDA UDI
510(k) Number
K012139 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Anaesthetic agent gas monitor, multiple FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Anaesthetic agent gas monitor, multiple

Vamos 2 by Drägerwerk AG & Co. KGaA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthetic agent gas monitor, multiple.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drägerwerk AG & Co. KGaA

Sources (1)

  • FDA UDI d2718cf0-aa93-4e08-82a5-7749372a7359 34 fields · synced May 30, 2026