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ViSi

FDA UDI

Class II (US FDA UDI)

by Sotera Wireless

Identity

Trade Name
ViSi FDA UDI
Generic Name
Patient monitoring system module, blood pressure, noninvasive FDA UDI
Device Name
Disposable Wrist Cradle, Medium (Qty 20) FDA UDI
Model / Reference
Disposable Wrist Cradle, Medium (Qty 20) FDA UDI
Description
Disposable Wrist Cradle, Medium (Qty 20) FDA UDI

Identifiers

Catalog Number
94-10173 FDA UDI
Primary DI / UDI-DI
00850733007346 FDA UDI
510(k) Number
K152341 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

Yes

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

Yes

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

ViSi by Sotera Wireless — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sotera Wireless

Sources (1)

  • FDA UDI c31366d8-8d4b-408e-a6dd-c0573dadfbce 35 fields · synced Jun 8, 2026