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Multi-Link™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
Multi-Link™ FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Device Name
Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™) FDA UDI
Model / Reference
2074817-001 FDA UDI
Description
Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™) FDA UDI

Identifiers

Catalog Number
2074817-001 FDA UDI
Primary DI / UDI-DI
10190752106130 FDA UDI
FDA Product Code
FMZ FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5400 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: General-purpose patient temperature probe, single-use

Multi-Link™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 9e459c07-027a-4124-9bd6-9503f4f17ae6 36 fields · synced Jun 1, 2026