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Vapor 3000

FDA UDI

Class II (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
Vapor 3000 FDA UDI
Generic Name
Isoflurane anaesthesia vaporizer FDA UDI
Model / Reference
M36500 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675301363 FDA UDI
510(k) Number
K971923 FDA UDI
FDA Product Code
CAD FDA UDI
GMDN Term
Isoflurane anaesthesia vaporizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5880 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: Isoflurane anaesthesia vaporizer

Vapor 3000 by Drägerwerk AG & Co. KGaA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Isoflurane anaesthesia vaporizer.

Cleared under the same submission

K971923 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI edb67aff-229b-48a8-9fb6-c050083b1117 34 fields · synced Jun 8, 2026