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Spotskan

FDA UDI

Class II (US FDA UDI)

by Skanray Technologies

Identity

Trade Name
Spotskan FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
Device Name
Multi-Parameter Spot Check Device FDA UDI
Model / Reference
F3-85-390-0335-13 FDA UDI
Description
Multi-Parameter Spot Check Device FDA UDI

Identifiers

Primary DI / UDI-DI
18904269450301 FDA UDI
FDA Product Code
MWI FDA UDI
DXN FDA UDI
GMDN Term
Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

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 Unsafe FDA UDI

Category: Automatic-inflation electronic sphygmomanometer, non-portable

Spotskan by Skanray Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic-inflation electronic sphygmomanometer, non-portable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skanray Technologies

Sources (1)

  • FDA UDI 04ef2ac7-f7ca-41c9-ace9-d1e2f37bc090 33 fields · synced May 30, 2026