Vital Signs™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name: Vital Signs™ FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: Vital Signs™ Elbow-Luer Port FDA UDI
Model / Reference: 5600EL FDA UDI
Description: Vital Signs™ Elbow-Luer Port FDA UDI

Identifiers

Catalog Number: 5600EL FDA UDI
Primary DI / UDI-DI: 10889483586730 FDA UDI
510(k) Number: K920885 FDA UDI
FDA Product Code: CAH FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5260 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Vital Signs™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K920885 also covers:

Vital Signs™ — Airlife, Inc.
Vital Signs™ — Airlife, Inc.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Airlife, Inc.

Sources (1)

FDA UDI e8c292b9-651e-4c73-9b41-63c244c6bd23 36 fields · synced Jun 8, 2026