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LMT nomag® IC 3.0

FDA UDI

Class II (US FDA UDI)

by LMT Medical Systems GmbH

Identity

Trade Name
LMT nomag® IC 3.0 FDA UDI
Generic Name
Transport infant incubator FDA UDI
Device Name
No description. FDA UDI
Model / Reference
0100025 FDA UDI
Description
No description. FDA UDI

Identifiers

Primary DI / UDI-DI
04260486610575 FDA UDI
510(k) Number
K062052 FDA UDI
FDA Product Code
FPL FDA UDI
GMDN Term
Transport infant incubator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5410 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 Conditional FDA UDI

Category: Transport infant incubator

LMT nomag® IC 3.0 by LMT Medical Systems GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transport infant incubator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4946bcaf-ff59-4ddd-b68d-0803a065041e 35 fields · synced May 30, 2026