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Lutech

FDA UDI

Class II (US FDA UDI)

by Lutech Industries

Identity

Trade Name
Lutech FDA UDI
Generic Name
Multiple vital physiological parameter monitoring system, clinical FDA UDI
Device Name
Multi-parameter patient monitor. 750-N-IC-P FDA UDI
Model / Reference
Datalys 750 FDA UDI
Description
Multi-parameter patient monitor. 750-N-IC-P FDA UDI

Identifiers

Primary DI / UDI-DI
B299750NICP0 FDA UDI
510(k) Number
K150691 FDA UDI
FDA Product Code
DPS FDA UDI
FLL FDA UDI
DQA FDA UDI
MWI FDA UDI
DXN FDA UDI
GMDN Term
Multiple vital physiological parameter monitoring system, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 FDA UDI
880.2910 FDA UDI
870.2700 FDA UDI
870.2300 FDA UDI
870.1130 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

No

FDA UDI

Category: Multiple vital physiological parameter monitoring system, clinical

Lutech by Lutech Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple vital physiological parameter monitoring system, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lutech Industries

Sources (1)

  • FDA UDI 81e2deca-a250-4999-959d-2c1617488b7c 34 fields · synced Jun 8, 2026