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Iradimed

FDA UDI

Class II (US FDA UDI)

by Iradimed Corporation

Identity

Trade Name
Iradimed FDA UDI
Generic Name
Anaesthetic agent gas monitor, multiple FDA UDI
Device Name
MRI Wireless Multi-Gas Unit w/O2 FDA UDI
Model / Reference
3886 FDA UDI
Description
MRI Wireless Multi-Gas Unit w/O2 FDA UDI

Identifiers

Catalog Number
3886 FDA UDI
Primary DI / UDI-DI
00856038001225 FDA UDI
510(k) Number
K172200 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Anaesthetic agent gas monitor, multiple FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 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

Yes

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 Conditional FDA UDI

Category: Anaesthetic agent gas monitor, multiple

Iradimed by Iradimed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthetic agent gas monitor, multiple.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab30792d-1d4b-45ad-bf1e-3cf34919a258 35 fields · synced Jun 8, 2026