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Slight Touch

FDA UDI

Class II (US FDA UDI)

by Nobel Supplies Group Llc

Identity

Trade Name
Slight Touch FDA UDI
Generic Name
Patient monitoring system module, blood pressure, noninvasive FDA UDI
Device Name
Automatic Arm Blood Pressure Monitor Large Cuff FDA UDI
Model / Reference
St-402 FDA UDI
Description
Automatic Arm Blood Pressure Monitor Large Cuff FDA UDI

Identifiers

Primary DI / UDI-DI
00862478000322 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Patient monitoring system module, blood pressure, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient monitoring system module, blood pressure, noninvasive

Slight Touch by Nobel Supplies Group Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, blood pressure, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Supplies Group Llc

Sources (1)

  • FDA UDI b53f035e-fcf6-4f70-a2c7-5ff6cb32ec48 34 fields · synced May 30, 2026