← Back to catalogue

UltraviewSL

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
UltraviewSL FDA UDI
Generic Name
Patient monitoring system module, multiple-gas FDA UDI
Device Name
MODULE, MS/SS DUAL CAPNOGRAPHY FDA UDI
Model / Reference
Ultraview SL® FDA UDI
Description
MODULE, MS/SS DUAL CAPNOGRAPHY FDA UDI

Identifiers

Catalog Number
91517 FDA UDI
Primary DI / UDI-DI
10841522112430 FDA UDI
510(k) Number
K031124 FDA UDI
FDA Product Code
CCL FDA UDI
MHX FDA UDI
CCK FDA UDI
GMDN Term
Patient monitoring system module, multiple-gas FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1720 FDA UDI
870.1025 FDA UDI
868.1400 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

Category: Patient monitoring system module, multiple-gas

UltraviewSL 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, multiple-gas.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1f17168e-c080-4cce-a861-20e483417a42 36 fields · synced May 30, 2026