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Vital Signs™

FDA UDI

Class II (US FDA UDI)

by AirLife Finland Oy

Identity

Trade Name
Vital Signs™ FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
Vital Signs™ Exhaust Line with Colder Fitting, 1 m/41 in FDA UDI
Model / Reference
8004462 FDA UDI
Description
Vital Signs™ Exhaust Line with Colder Fitting, 1 m/41 in FDA UDI

Identifiers

Catalog Number
8004462 FDA UDI
Primary DI / UDI-DI
10889483590058 FDA UDI
FDA Product Code
CCL FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1720 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

Yes

FDA UDI

Category: Gas-sampling/monitoring respiratory tubing, single-use

Vital Signs™ by AirLife Finland Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AirLife Finland Oy

Sources (1)

  • FDA UDI 1482142b-3d14-4192-b045-ed3edde8f1c5 35 fields · synced May 30, 2026