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Spacelabs Healthcare

FDA UDI

Class II (US FDA UDI)

by Spacelabs Healthcare (washington), Inc

Identity

Trade Name
Spacelabs Healthcare FDA UDI
Generic Name
Breathing circuit gas-flow sensor, reusable FDA UDI
Device Name
PATIENT FLOW SENSOR - SINGLE UNIT FDA UDI
Model / Reference
Flow Sensor FDA UDI
Description
PATIENT FLOW SENSOR - SINGLE UNIT FDA UDI

Identifiers

Catalog Number
10110090 FDA UDI
Primary DI / UDI-DI
10841522129759 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Breathing circuit gas-flow sensor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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: Breathing circuit gas-flow sensor, reusable

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

Similar devices

Also classified as Breathing circuit gas-flow sensor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 56387b7a-04c9-46db-be5d-495bfec1e117 34 fields · synced May 30, 2026