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Ultraview SL

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Ultraview SL FDA UDI
Generic Name
Patient monitoring system module, multifunction FDA UDI
Device Name
CABLE,ASSY ADAPTER MPT/SPO2 NELL FDA UDI
Model / Reference
ECG Cables & Leadwires FDA UDI
Description
CABLE,ASSY ADAPTER MPT/SPO2 NELL FDA UDI

Identifiers

Catalog Number
700-0014-00 FDA UDI
Primary DI / UDI-DI
10841522122637 FDA UDI
510(k) Number
K103142 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Patient monitoring system module, multifunction 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

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

Yes

FDA UDI

Category: Patient monitoring system module, multifunction

Ultraview SL by Spacelabs Healthcare (washington), Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, multifunction.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa7c9bc7-5f93-45cb-a019-fb6376124fae 36 fields · synced May 30, 2026