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AirLife™ Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2074816-001

by AirLife Finland Oy

Identity

Trade Name
AirLife™ Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™) EUDAMED
Airlife FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Device Name
AirLife™ Temperature monitoring EUDAMED
Infant Skin Temperature Probe, Single Patient Use FDA UDI
Model / Reference
2074816-001 EUDAMEDFDA UDI
Description
Infant Skin Temperature Probe, Single Patient Use FDA UDI

Identifiers

Catalog Number
2074816-001 FDA UDI
Primary DI / UDI-DI
10190752179608 EUDAMEDFDA UDI
Basic UDI-DI
0190752TDHEL1041UH EUDAMED
FDA Product Code
FMZ FDA UDI
EMDN Code
V03010201 TEMPERATURE MONITORING CUTANEOUS PROBES EUDAMED
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.5400 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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, reusable

AirLife™ Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™) by AirLife Finland Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as General-purpose patient temperature probe, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AirLife Finland Oy
EUDAMED SRN
FI-MF-000001482

Sources (2)

  • EUDAMED 6f76a822-03d3-4508-8365-baff9fab7c6f 61 fields · synced Jul 18, 2026
  • FDA UDI f7b01ede-0b04-437f-880d-3f710da578f8 36 fields · synced May 30, 2026